EP0257344A1 - Medicaments containing dipyridamol or mopidamol and O-acetylsalicylic acid, or its physiologically compatible salts, process for their manufacture and their use in combating the formation of thrombus - Google Patents
Medicaments containing dipyridamol or mopidamol and O-acetylsalicylic acid, or its physiologically compatible salts, process for their manufacture and their use in combating the formation of thrombus Download PDFInfo
- Publication number
- EP0257344A1 EP0257344A1 EP87111104A EP87111104A EP0257344A1 EP 0257344 A1 EP0257344 A1 EP 0257344A1 EP 87111104 A EP87111104 A EP 87111104A EP 87111104 A EP87111104 A EP 87111104A EP 0257344 A1 EP0257344 A1 EP 0257344A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- dipyridamole
- acetylsalicylic acid
- granules
- acid
- pellets
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
- A61K9/5084—Mixtures of one or more drugs in different galenical forms, at least one of which being granules, microcapsules or (coated) microparticles according to A61K9/16 or A61K9/50, e.g. for obtaining a specific release pattern or for combining different drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/60—Salicylic acid; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2072—Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
- A61K9/2086—Layered tablets, e.g. bilayer tablets; Tablets of the type inert core-active coat
- A61K9/209—Layered tablets, e.g. bilayer tablets; Tablets of the type inert core-active coat containing drug in at least two layers or in the core and in at least one outer layer
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4808—Preparations in capsules, e.g. of gelatin, of chocolate characterised by the form of the capsule or the structure of the filling; Capsules containing small tablets; Capsules with outer layer for immediate drug release
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
Definitions
- the invention relates to drug combinations consisting of dipyridamole or mopidamol and O-acetylsalicylic acid or their physiologically tolerable salts, processes for the preparation of these drug combinations and their use for the targeted prevention of thrombus formation.
- O-acetylsalicylic acid is known to act as an inhibitor of the aggregation of human platelets (see Br. J. Clin. Pharmac. 7 (1979) 283). It has been reported that O-acetylsalicylic acid inhibits the enzyme cyclooxygenase in the platelets and thus the biosynthesis of the thromboxane A2 which promotes aggregation. As the dosage increases, the antithrombotic effect of O-acetylsalicylic acid increases, but at the same time the inhibitory effect on the cyclooxygenase of the vascular walls also has a negative effect on the synthesis of the aggregation-inhibiting prostacyclin. It is suggested (cf.
- Dipyridamole (2,6-bis- (diethanolamino) -4,8-dipiperidino- (5,4-d) -pyrimidine) and mopidamole (2,6-bis- (diethanolamino) -8-piperidino- (5,4- d) -pyrimidine) are used clinically, inter alia, as antithrombotic and antiaggregatory agents and mopidamole also as metastasis-inhibiting agents.
- FR-B-2 368 272 describes a combination of dipyridamole and O-acetylsalicylic acid, preferably in a weight ratio of 4: 1 to 1: 4, which has a synergistic effect on the induced platelet aggregation. Since the two components are chemically incompatible with one another, it has been proposed to spatially separate them, e.g. by creating so-called layered tablets or coated core tablets.
- DE-Al-3 515 874 describes combination preparations containing pyrimidopyrimidines, in particular dipyridamole and / or mopidamol and O-acetylsalicylic acid or salts of these substances, the weight ratio of the pyrimidopyrimidine component to the O-acetylsalicylic acid component being greater than 0 , 5, and the pyrimidopyrimidine component is released first (bioavailable).
- This can e.g. B. can be achieved in that pharmaceutical carriers and excipients are used, which ensure a gradual release of the two components.
- the medical effect can only be achieved if the relative proportion of acetylsalicylic acid in the sequential (sequential or consecutive) dose is selected so that the weight ratio of pyrimido-pyrimidine to O-acetylsalicylic acid is not less than 0.5 .
- the weight ratio of pyrimidopyrimidine to O-acetylsalicylic acid should be more than 0.5 and up to 30. It should very preferably be between 0.6 and 3.
- a combination is released first of all from O-acetylsalicylic acid and, at different times, from pyrimidopyrimidine in the gastrointestinal tract. 15 to 90 minutes can be used as a time interval.
- the upper limit for the ratio of pyrimido pyrimidine to O-acetylsalicylic acid can be considered the number 100, primarily for practical reasons, but this upper limit should not be considered critical for the interaction of the two components.
- a limitation of the pyrimidopyrimidine content is e.g. B. for swallowable dosage forms, such as tablets or coated tablets, given that these forms become too bulky when the pyrimidopyrimidine content is increased further.
- the two components pyrimidopyrimidine and O-acetylsalicylic acid can be present as a mixture which is particularly suitable for the production of instant forms, the two components being separated from one another by application of a suitable protective layer and thus being stable in storage.
- the component O-acetylsalicylic acid is not free from traces of acetic acid which arise from the cleavage of the acetylsalicylic acid during storage.
- the free acetic acid reacts with the dipyridamole to form hygroscopic salts and dipyridamole-acetic acid esters, which lead to the deterioration of the dipyridamole.
- dipyridamole in the form of pellets or granules with a gastric juice-insoluble but intestinal juice-soluble lacquer and / or the acetylsalicylic acid kernels or tablets with an acetic acid-tight coating, which dissolves very quickly in the gastric juice. The same applies to mopidamol.
- dipyridamole granules separating granules and acetylsalicylic acid granules separately and then compressing them into three-layer tablets;
- a pyrimidopyrimidine granulate can, however, also be filled into a capsule together with a coated tablet or film-coated tablet containing the O-acetylsalicylic acid.
- the pyrimidopyrimidine blood level is of a consistently high value, it is advantageous to start from pyrimidopyrimidine pellets, which enable a time-controlled and pH-controlled release of this active ingredient, and to process these together with the O-acetylsalicylic acid to give corresponding medicinal forms. It can also be advantageous here to produce compacts of O-acetylsalicylic acid with an appropriate covering through a film layer and to combine them with the pyrimidopyrimidine pellets.
- the pyrimidopyrimidine pellets can be coated with a layer which retards the release of this active ingredient and the cores containing O-acetylsalicylic acid with a layer soluble in gastric juice.
- dipyridamole pellets with a controlled release of the active ingredient it is particularly advantageous to use those which have been prepared in accordance with the recipes described in DE-A-3 000 989.1. These pellets have a coating that acts as a dialysis membrane and releases the active ingredient dipyridamole in combination with acids in the gastrointestinal tract in a controlled manner.
- the structure and composition of the pellets leads to the release of dissolved dipyridamole in the form of its salts.
- Retard pellets produced in this way lead to complete absorption of the dipyridamole from the gastrointestinal tract.
- uniform blood levels can be achieved over 8 to 10 hours while avoiding blood level peaks, as frequently occur with the commercially available dipyridamole-acetylsalicylic acid forms (for example according to FR-B-2 368 272).
- the blood level peaks observed in the forms according to this French patent originate from the fact that dipyridamole is only partially and individually absorbed to different degrees.
- the blood level values drop below the effective range after a short time or are sometimes not reached (with a so-called “non-absorber”);
- O-acetylsalicylic acid achieves its pharmacological activity in every patient.
- a preferred subject of the present invention thus relates to pharmaceutical forms consisting of dipyridamole and / or mopidamol in combination with a physiologically acceptable acid, at least 1 val acid per 1 mol dipyridamole or mopidamol, surrounded by a covering which consists of 50 to 100% acid-insoluble , intestinal juice-soluble paints and consists of 50 to 0% gastric and intestinal juice-insoluble paints, this component being in the form of granules or pellets, and the component O-acetylsalicylic acid, which is preferably provided with a gastric juice-soluble coating and is preferably in the form of a tablet or film-coated tablet, the two components must be in a weight ratio of at least 4.5.
- While preferred forms according to DE-Al-3 515 874 have a weight ratio of pyrimidopyrimidine to O-acetylsalicylic acid between 0.6 and 1.5 (further ratios are not described by examples), these weight ratios in the case of the present invention are above 4 , 5, preferably 8 to 100.
- the pharmaceutical forms contain between 10 and 675 mg dipyridamole and / or mopidamol and between 1 and 150 mg O-acetylsalicylic acid.
- Preferred forms for dipyridamole and mopidamole contain between 75 and 400 mg of this active ingredient, very preferred forms between 75 and 200 mg in addition to 5 to 80 mg and 5 to 40 mg of O-acetylsalicylic acid.
- 2 to 3 of these dose units are given per day, depending on the severity of the case, deviations from this dose up and down are possible.
- the dosage to be used will of course also depend on other factors, e.g. B. from Age, weight, general state of health of the patient to be treated, the severity of the symptoms or the disease.
- the pharmaceutical preparation forms according to the invention optionally also contain other customary excipients and / or auxiliaries and are prepared by processes which are customary per se.
- carriers and / or auxiliaries z.
- dipyridamole granulate for. B. dipyridamole with an organic edible acid, such as fumaric acid, tartaric acid, citric acid, succinic acid, malic acid and with binders and / or adhesives, such as. B. polyvinylpyrrolidone, mixed with a lubricant such as. B. magnesium stearate, the mixture is subsequently compressed, for. B. with the help of a roller compactor, and broken up into granules, for. B. using a dry pelletizer with a downstream screening device.
- an organic edible acid such as fumaric acid, tartaric acid, citric acid, succinic acid, malic acid and with binders and / or adhesives, such as. B. polyvinylpyrrolidone
- a lubricant such as. B. magnesium stearate
- Dipyridamole pellets are preferably produced using starter cores, which are advantageously made from an organic edible acid, e.g. B. from rounded tartaric acid crystals exist (diameter of the starter cores 0.5 to 0.9 mm), on which in a kettle a suspension of dipyridamole in an alcohol or alcohol / water mixture and from a binder, such as. B. polyvinylpyrrolidone is sprayed on until the resulting active substance pellets contain the prescribed amount of dipyridamole (the pellets then have a diameter between 0.9 and 1.5 mm).
- starter cores which are advantageously made from an organic edible acid, e.g. B. from rounded tartaric acid crystals exist (diameter of the starter cores 0.5 to 0.9 mm), on which in a kettle a suspension of dipyridamole in an alcohol or alcohol / water mixture and from a binder, such as. B. polyvinylpyrrolidone is sprayed on until the
- a varnish which consists of 50 to 100% acid-insoluble, intestinal juice-soluble varnishes and 50 to 0% of gastric and intestinal juice-insoluble varnishes.
- a varnish made of methacrylic acid / methacrylic acid ester copolymers (Eudragit S®) and hydroxypropylmethyl cellulose phthalate (HP 55®), which contains plasticizers and fillers, e.g. B. talc can be added.
- intestinal juice-soluble coating components are also cellulose acetate phthalate, lulosephthalat Ethylcel, hydroxypropylmethylcellulose succinate, cellulose acetate succinate, hydroxypropylmethyl cellulose, cellulose acetate hexahydrophthalate, hydroxypropylmethyl cellulose trimellitate, methacrylic acid-methacrylic acid copolymer (acid number 300 to 330, Eudragit L®), or mixtures of these substances in question.
- Intestinal juice and gastric juice-insoluble varnishes as admixtures can be: varnishes based on acrylate or methacrylate (Eudragit retard S® and Eudragit retard L®), also in combination with up to 14% by weight of ethyl cellulose.
- Dipyridamole (and / or mopidamole) pellets can also be obtained by placing a powder mixture of dipyridamole (and / or mopidamole) and the calculated amount of an organic edible acid (e.g. in an extruder (e.g. twin screw extruder)). Fumaric acid) and binder and possibly other auxiliaries, an organic solvent is added and the mixture is mixed. The moistened mass is expressed in the form of spaghetti, which are rounded on a fast rotating plate to high-density pellets. The pellets are then dried and, if appropriate, coated with a retarding lacquer as described above.
- an organic edible acid e.g. in an extruder (e.g. twin screw extruder)
- Fumaric acid) and binder and possibly other auxiliaries an organic solvent is added and the mixture is mixed.
- the moistened mass is expressed in the form of spaghetti, which are rounded on a fast rotating plate to high-density pellets.
- the pellets
- O-acetylsalicylic acid can be used once in the form of pressed cores, which are covered with an insulating cover layer, or in the form of film-coated tablets.
- the moldings are made from O-acetylsalicylic acid, flow and Lubricants and carriers and / or diluents, such as. B. flowable lactose, microcrystalline cellulose, dried corn starch, aluminum or magnesium stearate, obtained in a manner known per se by producing and pressing a corresponding granulate.
- the cores are coated, if necessary in several steps, with a coating suspension which, for. B. from sugars (such as sucrose), gum arabic, talc and similar substances.
- a typical three-layer tablet is obtained, for example, by adding a pyrimidopyrimidine granulate, an O-acetylsalicylic acid granulate and a separating granulate which, for. B. is made of lactose, microcrystalline cellulose and polyvinylpyrrolidone and contains a lubricant, is pressed by means of a special tablet press with 3 filling funnels and 3 pressing stations so that the neutral separating layer lies between the two pressed active ingredients.
- the combination according to the invention is used as an antithrombotic agent which inhibits blood platelet aggregation and the effect of metastases in humans and animals; the combination prevents the formation and maintenance of venous and arterial blood clots, it thus prevents transient ischemic attacks and serves as a preventive measure to prevent heart attacks and strokes. It is well-suited for preventing the formation and maintenance of a thrombus in the presence of arteriosclerosis or after surgery or other conditions associated with thrombosis; in use, however, the typical properties of the individual components also come into effect, e.g. B. there is an improved O2 supply to the heart muscle and inhibition of inflammatory processes, furthermore to pain relief.
- the staggered oral administration of the substances according to the above-mentioned European application was such that dipyridamole was first given 90 minutes before the administration of O-acetylsalicylic acid, the latter 60 minutes before the thrombus was set and the measurements began; in other words, dipyridamole was given 150 minutes and O-acetylsalicylic acid 60 minutes before the start of the experiment.
- the animals were given approximately 60 mg / kg of Nembutal i.p. anesthetized, her abdomen opened and part of the mesentery dislodged to the outside and washed over with physiological, heated nutrient solution during the course of the measurements.
- a platinum electrode was placed on an outer vessel wall of the mesentery under intravital microscopic observation.
- a counter electrode was inserted under the mesentery.
- a fixed combination between created DC voltage (150 V) and current (1.5 mA) in one pulse with a predetermined length (100 ms) leads to a reproducible formation of a thrombus in a venule of approx. 300 ⁇ m diameter, which usually closes 80% of the vessel diameter.
- the size of the thrombus is measured at intervals of 10 seconds, later 30 seconds in a time range up to 20 minutes after irritation of the vessel, and is given as the thrombus size (perpendicular to the vessel wall) as a percentage of the inner diameter of the vessel.
- a rapidly formed thrombus is generally held responsible for an existing injury or pathological change in the vessel wall.
- medication which inhibits thrombus formation it is to be expected that the thrombus formed will not reach the size of 85% of the vessel diameter achieved in the control group. This is the only way to prevent the uninhibited formation of a thrombus from obstructing blood flow, which usually has serious consequences from the ischemic damage that then arises (e.g. heart attack, stroke).
- FIGS. 1 and 2 show the time course of the thrombus size according to electrical Thrombus setting for a combination according to the above-mentioned European patent application No. 85 108 761.9 ( Figure 1) and a combination according to the invention ( Figure 2).
- Figure 1 shows the course of the thrombus size within 20 minutes after setting the thrombus after an oral administration of 5 mg / kg O-acetylsalicylic acid 60 minutes before the measurement and an oral administration of 5 mg / kg dipyridamole 150 minutes before the measurement .
- the size of the thrombus remained approximately 85% during the first half of the observation period, to decrease slightly in the second half, while in the treated group the size of the thrombus initially assumed values close to that of the control attempt within the first 30 seconds in order to decrease more in the further course of the experiment.
- FIG. 2 A clearly different time course is shown in Figure 2.
- a control group was compared with a group that according to the invention received 5 mg / kg of dipyridamole orally and 0.05 mg / kg of O-acetylsalicylic acid simultaneously 60 minutes before the start of the measurements.
- the treated group showed a clearly inhibited formation of the thrombus at the beginning and in the first period of the experiment, which at the beginning of the experiment assumed the values that in the case of the treated group of Figure 1 only in the second third of the Attempt is achieved.
- Figures 3 to 6 summarize the percentage thrombus sizes in individual time periods and compare them with each other.
- Columns A represent the thrombus sizes of the control group, i.e. the control group thrombus size was set to 100%.
- Columns B show the thrombus sizes of a combination of 5 mg / kg dipyridamole and 5 mg / kg O-acetylsalicylic acid according to the curve in Figure 1
- columns C show the thrombus sizes after prior application of 2.5 mg / kg O-acetylsalicylic acid
- the columns D with prior application of 5 mg / kg dipyridamole and the columns E after prior application of the combination according to the invention of 5 mg / kg dipyridamole and 0.05 mg / kg O-acetylsalicylic acid according to the curve in Figure 2
- the columns F of 2 mg / kg of dipyridamole and 0.05 mg / kg of O-acetylsalicylic acid (all applications were
- Figure 3 shows the percentage reduction in the 85% occlusion from 10 seconds to 1 minute after irritation of the vessel compared to the controls used at 100%.
- the size of the thrombus set during the electrical stimulation is already reduced by approximately 20% (practically already in statu nascendi); after administration of the previously known combination (column B), however, only by about 5%; this means that the thrombus formation is already significantly prevented when the combination according to the invention is administered.
- Figure 4 shows the same conditions in the time range 2 to 4 minutes from the irritation.
- the thrombus size generally decreases, the reduction is most pronounced in the combination according to the invention.
- Figure 5 shows the conditions in the time range 5 to 10 minutes after stimulation
- Figure 6 shows the time range 10 to 20 minutes. Only after about 15 minutes is a reduction in thrombus size achieved in the previously known combination, which corresponds to that achieved by the combination according to the invention. O-acetylsalicylic acid and dipyridamole alone do not significantly reduce thrombus size. Comparing the percentage reductions in Figure 6 in particular, you can see that the acetylsalicylic acid-dipyridamole combinations are superadditive or synergistic effects.
- the pattern of the flow reduction cycles is determined before administration of the active ingredient for comparison purposes. From the difference in the flow reduction rate and the amplitude of the cyclic flow oscillation, a flow pattern is constructed with a computer, which reflects the increase in free flow at any time after the active substance has been administered. Mechanically induced thrombus embolizations are negatively assessed compared to spontaneous thrombus embolizations (i.e. there is no or, if necessary, a positive correction). From these corrected curves, the computer calculates the parameter "free flow" for 20 or 30 minute intervals before and after the administration of the active ingredient. In order to minimize topical effects, which can occur with oral administration of acetylsalicylic acid, the active substances were administered as a bolus in the mesenteric vein.
- Figure 11 shows roughly the conditions for a known combination (Asasantin®); it can be seen that this is significantly less effective than the combinations according to the invention. Since comparatively high concentrations of acetylsalicylic acid are always used in the previously known combinations, an increased risk of bleeding has also been repeatedly pointed out.
- the combinations according to the invention surprisingly show a significantly better effect with a significantly reduced concentration of acetylsalicylic acid, which means a very significant reduction or even avoidance of the risk of bleeding.
- the preferred dose (in rabbits) is 50: 1 (dipyridamole to acetylsalicylic acid).
- the superiority of the treatment with a ratio of 100: 1 over that with a ratio of 10: 1 in preventing thrombus formation confirms the results mentioned above in experiments with the rat mesenteric vein model.
- 35 kg of dipyridamole, 30 kg of fumaric acid and 5 kg of polyvinylpyrrolidone are mixed in a cube mixer for 15 minutes.
- 0.4 kg of magnesium stearate are mixed in and mixed again for 5 minutes.
- the mixture is passed through a roller compactor, which is followed by a dry pelletizer with a screening device.
- the fraction from 0.4 to 1.0 mm in diameter is used.
- O-acetylsalicylic acid 35 kg are mixed with 3.3 kg of flowable lactose, 12.5 kg of microcrystalline cellulose, 9 kg of dried corn starch and 0.5 kg of aluminum stearate in a cube mixer for 15 minutes and then mixed with 90 mg, biconvex tablets pressed with a diameter of 5.5 mm.
- the quantity of granules corresponding to 175 mg of dipyridamole is filled into a hard gelatin capsule of size 1 and the dragée containing 35 mg of O-acetylsalicylic acid is then placed on top.
- the weight ratio of dipyridamole to O-acetylsalicylic acid is 5.
- Capsules containing dipyridamole depot forms in addition to a dragée with O-acetylsalicylic acid
- pellets are sprayed with a lacquer consisting of methacrylic acid / methyl methacrylate copolymer (trade name Eudragit S) and hydroxypropylmethyl cellulose phthalate (trade name HP 55) in a weight ratio of 85:15 to 50:50.
- the organic paint solutions also contain plasticizers and talc.
- Two pellet components with 5 and 7% casing content and different ratios of the lacquer components are sprayed within the stated limits. The two components are mixed so that they give the following in vitro release:
- acetylsalicylic acid cores are produced by pressing the following mixture: O-acetylsalicylic acid 25.0% by weight Lactose 53.0% by weight Microcrystalline cellulose 11.0% by weight Corn starch, dried 8.6% by weight Silicon dioxide 3.0% by weight Aluminum stearate 0.4% by weight
- these kernels are coated with the coating suspension mentioned until they weigh 120 mg after thorough drying.
- the weight ratio of dipyridamole to O-acetylsalicylic acid is 8.
- Capsules containing a dipyridamole depot form next to a dragée with O-acetylsalicylic acid
- a powder mixture containing dipyridamole and an organic solvent are metered in in the correct ratio and mixed together.
- the moistened mass is expressed in the form of spaghetti, which are rounded into highly compacted pellets in a container with a rapidly rotating base plate.
- the pellets are then dried in a drying cabinet.
- a pellet quantity corresponding to 450 mg dipyridamole and a dragée containing 5 mg acetylsalicylic acid are filled into a capsule of size OO.
- the weight ratio of dipyridamole to O-acetylsalicylic acid is 90.
- a powder mixture of 80% dipyridamole, 10% hydroxypropylmethyl cellulose (high polymer) and 9.5% hydroxypropyl cellulose (high polymer) are moistened with ethanol in a granulator and granulated through a sieve with a mesh size of 1.5 mm. After drying and sieving, 0.5% magnesium stearate is mixed in (percentages in% by weight).
- a mixture of 50% lactose and 45% microcrystalline cellulose is moistened with 4.5% polyvinylpyrrolidone, dissolved in water.
- the granulate sieved through a sieve with a mesh size of 1 mm is dried and mixed with 0.5% aluminum stearate (percentages in% by weight).
- the granules are metered in on a special tablet press with 3 filling funnels and 3 pressing stations so that a tablet with 400 mg dipyridamole and 80 mg acetylsalicylic acid is formed.
- the neutral layer between the two active substances weighs 50 mg.
- the tablet in oblong form (17 ⁇ 6.8 mm) is dedusted well, dried and sealed in aluminum / aluminum blister strips.
- the weight ratio of dipyridamole to O-acetylsalicylic acid is 5.
- a mixture of 30% dipyridamole, 63% fumaric acid and 6% polyvinylpyrrolidone is moistened with ethanol and sieved through a sieve with a mesh size of 1.5 mm. After drying, 1% of magnesium stearate is added and the granules are compacted on a roller compactor equipped with a dry granulator with a sieve.
- the fraction of the grain size from 0.4 to 1.25 mm is used further (percentages in% by weight).
- the active ingredient release of the granules containing dipyridamole is pH-independent:
- the weight ratio of dipyridamole to O-acetylsalicylic acid is 20.
- 35 kg of mopidamol, 20 kg of fumaric acid and 5 kg of polyvinylpyrrolidone are mixed in a cube mixer for 15 minutes.
- 0.4 kg of magnesium stearate are mixed in and mixed again for 5 minutes.
- the mixture is passed through a roller compactor, which is followed by a dry pelletizer with a screening device.
- the fraction from 0.4 to 1.0 mm in diameter is used.
- O-acetylsalicylic acid 35 kg are mixed with 3.3 kg of flowable lactose, 12.5 kg of microcrystalline cellulose, 9 kg of dried corn starch and 0.5 kg of aluminum stearate in a cube mixer for 15 minutes and then mixed with 90 mg, biconvex tablets pressed with a diameter of 5.5 mm.
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Abstract
Description
Die Erfindung betrifft Arzneimittelkombinationen, bestehend aus Dipyridamol oder Mopidamol und O-Acetylsalicylsäure bzw. deren physiologisch verträglichen Salzen, Verfahren zur Herstellung dieser Arzneimittelkombinationen und deren Verwendung zur gezielten Verhütung von Thrombusbildungen.The invention relates to drug combinations consisting of dipyridamole or mopidamol and O-acetylsalicylic acid or their physiologically tolerable salts, processes for the preparation of these drug combinations and their use for the targeted prevention of thrombus formation.
Von O-Acetylsalicylsäure ist bekannt, daß es als Hemmstoff der Aggregation menschlicher Blutplättchen entgegenwirkt (vgl. Br. J. Clin. Pharmac. 7 (1979) 283). Es wurde berichtet, daß O-Acetylsalicylsäure das Enzym Cyclooxygenase in den Blutplättchen und damit die Biosynthese des die Aggregation fördernden Thromboxan A₂ hemmt. Mit steigender Dosierung nimmt zwar die antithrombotische Wirkung der O-Acetylsalicylsäure zu, gleichzeitig aber auch die hemmende Wirkung auf die Cyclooxygenase der Gefäßwände, wodurch mittelbar auch die Synthese des die Aggregation hemmenden Prostazyklins negativ beeinflußt wird. Es wird nahegelegt (vgl. Lancet, III (1979) 1213, Prostaglandins and Medicine 4 (1980) 439) mit möglichst niedrigen Dosierungen an Acetylsalicylsäure auszukommen. Andererseits wird aber empfohlen (Prostaglandins, Leukotriens and Medicin 12 (1983) 235), höhere Dosierungen zu verwenden, da mit steigender Dosierung die antithrombotische Wirkung der Acetylsalicyclsäure auch dann noch erhöht wird, wenn die Prostazyklin- und Thromboxan-Biosynthese bereits gehemmt wird.O-acetylsalicylic acid is known to act as an inhibitor of the aggregation of human platelets (see Br. J. Clin. Pharmac. 7 (1979) 283). It has been reported that O-acetylsalicylic acid inhibits the enzyme cyclooxygenase in the platelets and thus the biosynthesis of the thromboxane A₂ which promotes aggregation. As the dosage increases, the antithrombotic effect of O-acetylsalicylic acid increases, but at the same time the inhibitory effect on the cyclooxygenase of the vascular walls also has a negative effect on the synthesis of the aggregation-inhibiting prostacyclin. It is suggested (cf. Lancet, III (1979) 1213, Prostaglandins and Medicine 4 (1980) 439) to get by with the lowest possible doses of acetylsalicylic acid. On the other hand, however, it is recommended (Prostaglandins, Leukotriens and Medicin 12 (1983) 235) to use higher doses, since the dose increases the antithrombotic effect of acetylsalicyclic acid is increased even if the prostacyclin and thromboxane biosynthesis is already inhibited.
Dipyridamol (2,6-Bis-(diäthanolamino)-4,8-dipiperidino-(5,4-d)-pyrimidin) und Mopidamol (2,6-Bis-(diäthanolamino)-8-piperidino-(5,4-d)-pyrimidin) werden klinisch unter anderem als antithrombotisch und antiaggregatorisch wirkende und Mopidamol auch als Metastasen-inhibierende Wirkstoffe eingesetzt.Dipyridamole (2,6-bis- (diethanolamino) -4,8-dipiperidino- (5,4-d) -pyrimidine) and mopidamole (2,6-bis- (diethanolamino) -8-piperidino- (5,4- d) -pyrimidine) are used clinically, inter alia, as antithrombotic and antiaggregatory agents and mopidamole also as metastasis-inhibiting agents.
Durch die FR-B-2 368 272 wird eine Kombination aus Dipyridamol und O-Acetylsalicylsäure, vorzugsweise in einem Gewichtsverhältnis von 4:1 bis 1:4, beschrieben, welche eine synergistische Wirkung auf die induzierte Thrombocytenaggregation ausübt. Da die beiden Komponenten miteinander chemisch unverträglich sind, wurde vorgeschlagen, diese räumlich voneinander zu trennen, z.B. durch Schaffung sogenannter Schichttabletten oder Mantel-Kern-Tabletten.FR-B-2 368 272 describes a combination of dipyridamole and O-acetylsalicylic acid, preferably in a weight ratio of 4: 1 to 1: 4, which has a synergistic effect on the induced platelet aggregation. Since the two components are chemically incompatible with one another, it has been proposed to spatially separate them, e.g. by creating so-called layered tablets or coated core tablets.
Bekannt ist das Präparat Asasantin® der Firma Dr. Karl Thomae GmbH, Biberach/Riss, enthaltend 330 mg O-Acetylsalicylsäure neben 75 mg Dipyridamol, bekannt wurden auch Kombinationsmöglichkeiten anderer Pyrimidopyrimidine mit der Acetylsalicylsäure in Verhältnissen von 0,5 und darunter (vgl. FR-B-2 390 959).The Asasantin® preparation from Dr. Karl Thomae GmbH, Biberach / Riss, containing 330 mg O-acetylsalicylic acid in addition to 75 mg dipyridamole, combinations of other pyrimidopyrimidines with acetylsalicylic acid in ratios of 0.5 and below were also known (cf. FR-B-2 390 959).
Die DE-Al-3 515 874 beschreibt Kombinationspräparate, enthaltend Pyrimido-pyrimidine, insbesondere Dipyridamol und/oder Mopidamol und O-Acetylsalicylsäure oder Salze dieser Stoffe, wobei das Gewichtsverhältnis der Pyrimido-pyrimidin-Komponente zu der O-Acetylsalicylsäure-Komponente größer als 0,5 ist, und die Pyrimido-pyrimidin-Komponente zuerst freigesetzt (bioverfügbar) wird. Dies kann z. B. dadurch erreicht werden, daß pharmazeutische Träger und Hilfsstoffe verwendet werden, die für eine zeitlich abgestufte Freisetzung der beiden Komponenten sorgen. Nach den dort ge machten Angaben läßt sich der medizinische Effekt nur dann erzielen, wenn der relative Acetylsalicylsäure-Anteil bei der zeitlich aufeinanderfolgenden (sequentiellen bzw. konsekutiven) Gabe so gewählt ist, daß ein Gewichtsverhältnis von Pyrimido-pyrimidin zu O-Acetylsalicylsäure von 0,5 nicht unterschritten wird. Das Gewichtsverhältnis von Pyrimido-pyrimidin zu O-Acetylsalicylsäure soll mehr als 0,5 und bis zu 30 betragen. Ganz bevorzugt soll es zwischen 0,6 und 3 liegen. Zwischen der Freisetzung der Pyrimido-pyrimidin-Komponente und der O-Acetylsalicylsäure-Komponente muß ein Zeitabstand von 15 Minuten bis zu 2 Stunden, vorzugsweise von 30 Minuten bis zu 90 Minuten liegen, ganz bevorzugt zwischen 40 und 70 Minuten. Nach den dortigen Angaben wird es, wegen eines überadditiven Effektes, möglich, die Dosierung der Einzelkomponenten entscheidend zu erniedrigen, und zwar weit unter die Dosierungen, die man zur Erzielung des gleichen Effektes mit Einzelgaben Acetylsalicylsäure oder Pyrimido-pyrimidin oder mit der kombinierten gleichzeitigen Verabreichung von Acetylsalicylsäure und Pyrimido-pyrimidin benötigen würde.DE-Al-3 515 874 describes combination preparations containing pyrimidopyrimidines, in particular dipyridamole and / or mopidamol and O-acetylsalicylic acid or salts of these substances, the weight ratio of the pyrimidopyrimidine component to the O-acetylsalicylic acid component being greater than 0 , 5, and the pyrimidopyrimidine component is released first (bioavailable). This can e.g. B. can be achieved in that pharmaceutical carriers and excipients are used, which ensure a gradual release of the two components. According to the ge As stated, the medical effect can only be achieved if the relative proportion of acetylsalicylic acid in the sequential (sequential or consecutive) dose is selected so that the weight ratio of pyrimido-pyrimidine to O-acetylsalicylic acid is not less than 0.5 . The weight ratio of pyrimidopyrimidine to O-acetylsalicylic acid should be more than 0.5 and up to 30. It should very preferably be between 0.6 and 3. Between the release of the pyrimidopyrimidine component and the O-acetylsalicylic acid component there must be a time interval of 15 minutes to 2 hours, preferably 30 minutes to 90 minutes, very preferably between 40 and 70 minutes. According to the information given there, because of a super-additive effect, it is possible to significantly reduce the dosage of the individual components, and far below the dosages that can be achieved with single doses of acetylsalicylic acid or pyrimidopyrimidine or with the combined simultaneous administration of to achieve the same effect Acetylsalicylic acid and pyrimidopyrimidine would need.
Es wurde nun gefunden, daß eine Kombination bestehend aus Dipyridamol und/oder Mopidamol bzw. deren physioligisch verträglichen Salzen und O-Acetylsalicylsäure bzw. ihrer physiologisch verträglichen Salzen, welche die beiden Komponenten in einem Gewichtsverhältnis von größer als 4,5, bevorzugt aber größer als 5 enthält und die beiden Komponenten gleichzeitig im Magen-Darm-Trakt freisetzt, die Thrombusbildung signifikant reduziert bzw. verhindert und gleichzeitig einen einmal gebildeten Thrombus schneller auflöst, als dieses durch die natürliche Thrombolyse der Fall wäre. In manchen Fällen, die von der Ursache der Thrombusbildung abhängen, kann es sogar von Vorteil sein, wenn einer solchen Kombination zuerst die O-Acetylsalicylsäure und, zeitlich versetzt, das Pyrimido-pyrimidin im Magen-Darm-Trakt freigesetzt werden. Als Zeitabstand kommen hierfür 15 bis 90 Minuten in Frage. Als oberer Grenzwert für das Verhältnis von Pyrimido- pyrimidin zu O-Acetylsalicylsäure kann, in erster Linie aus praktischen Gründen, die Zahl 100 angesehen werden, diese Obergrenze ist aber für das Zusammenwirken der beiden Komponenten als nicht kritsch zu betrachten. Eine Begrenzung des Pyrimido-pyrimidin-Gehalts ist z. B. für schluckbare Arzneiformen, wie Tabletten oder Dragées, dadurch gegeben, daß bei einer weiteren Erhöhung des Pyrimido-pyrimidin-Gehalts diese Formen zu voluminös werden.It has now been found that a combination consisting of dipyridamole and / or mopidamol or their physiologically tolerable salts and O-acetylsalicylic acid or their physiologically tolerable salts, which the two components in a weight ratio of greater than 4.5, but preferably greater than 5 contains and simultaneously releases the two components in the gastrointestinal tract, significantly reduces or prevents thrombus formation and at the same time dissolves a thrombus once formed, than would be the case through natural thrombolysis. In some cases, which depend on the cause of the thrombus formation, it may even be of advantage if such a combination is released first of all from O-acetylsalicylic acid and, at different times, from pyrimidopyrimidine in the gastrointestinal tract. 15 to 90 minutes can be used as a time interval. As the upper limit for the ratio of pyrimido pyrimidine to O-acetylsalicylic acid can be considered the
Die beiden Komponenten Pyrimido-pyrimidin und O-Acetylsalicylsäure können als ein Gemisch vorliegen, welches sich für die Herstellung von Instant-Formen besonders eignet, wobei die beiden Komponenten durch Anbringung einer geeigneten Schutzschicht voneinander getrennt und damit lagerstabil sind. Bekanntlich ist die Komponente O-Acetylsalicylsäure nicht frei von Spuren an Essigsäure, die aus der Spaltung der Acetylsalicylsäure während der Lagerung entstehen. Die freie Essigsäure reagiert mit dem Dipyridamol unter Bildung hygroskopischer Salze und Dipyridamol-Essigsäure-Ester, die zum Verderb des Dipyridamols führen. Man kann diese Vorgänge am Dipyridamol dadurch unterbinden, daß man die eine oder die andere oder beide Komponenten mit einer Trennschicht versieht. So versieht man z. B. Dipyridamol in Form von Pellets oder Granulaten mit einem magensaftunlöslichen, aber darmsaftlöslichen Lack und/oder die Acetylsalicylsäure-Kerne oder -Tabletten mit einem essigsäuredichten Überzug, der im Magensaft sehr schnell aufgelöst wird. Gleiches gilt auch für das Mopidamol.The two components pyrimidopyrimidine and O-acetylsalicylic acid can be present as a mixture which is particularly suitable for the production of instant forms, the two components being separated from one another by application of a suitable protective layer and thus being stable in storage. As is known, the component O-acetylsalicylic acid is not free from traces of acetic acid which arise from the cleavage of the acetylsalicylic acid during storage. The free acetic acid reacts with the dipyridamole to form hygroscopic salts and dipyridamole-acetic acid esters, which lead to the deterioration of the dipyridamole. These processes on the dipyridamole can be prevented by providing one or the other or both components with a separating layer. So you provide z. B. dipyridamole in the form of pellets or granules with a gastric juice-insoluble but intestinal juice-soluble lacquer and / or the acetylsalicylic acid kernels or tablets with an acetic acid-tight coating, which dissolves very quickly in the gastric juice. The same applies to mopidamol.
Man kann aber auch beispielsweise ein Dipyridamolgranulat, ein Trenngranulat und ein Acetylsalicylsäuregranulat getrennt herstellen und anschließend zu Dreischicht-Tabletten verpressen; ein Pyrimido-pyrimidin-Granulat läßt sich aber auch, zusammen mit einem eine Schutzschicht tragenden Dragée bzw. Filmtablette, enthaltend die O-Acetylsalicylsäure, in eine Kapsel einfüllen. Legt man dagegen einen besonderen Wert auf einen gleichmäßig hohen Pyrimido-pyrimidinblutspiegel, so geht man vorteilhafterweise von Pyrimido-pyrimidin-Pellets aus, welche eine zeitlich und pH-gesteuerte Abgabe dieses Wirkstoffes ermöglichen, und verarbeitet diese zusammen mit der O-Acetylsalicylsäure zu entsprechenden Arzneiformen. Hierbei kann es auch vorteilhaft sein, Preßlinge der O-Acetylsalicylsäure mit einer entsprechenden Abdeckung durch eine Filmschicht herzustellen und diese mit den Pyrimido-pyrimidin-Pellets zu kombinieren. Will man eine zeitlich vorversetzte Abgabe der O-Acetylsalicylsäure erreichen, so kann man die Pyrimido-pyrimidin-Pellets mit einer, die Abgabe dieses Wirkstoffes retardierenden Schicht und die O-Acetylsalicylsäure enthaltende Kerne mit einer magensaftlöslichen Schicht überziehen. Im Falle von Dipyridamol-Pellets mit einer kontrollierten Freigabe des Wirkstoffes ist es besonders vorteilhaft, solche zu verwenden, welche gemäß den in der DE-A-3 000 989.1 beschriebenen Rezepturen hergestellt wurden. Diese Pellets besitzen einen Überzug, der als Dialysemembran wirkt und den Wirkstoff Dipyridamol in Verbindung mit Säuren im Magen-Darm-Trakt in geregelter Weise retardiert abgibt. Der Aufbau und die Zusammensetzung der Pellets führt zur Freigabe gelösten Dipyridamols in Form seiner Salze. So hergestellte Retard-Pellets führen zu einer vollständigen Resorption des Dipyridamols aus dem Magen-Darm-Trakt. Man erreicht damit gleichmäßige Blutspiegel über 8 bis 10 Stunden unter Vermeidung von Blutspiegelspitzen, wie sie bei den sich im Handel befindlichen Dipyridamol-Acetylsalicylsäure-Formen (z.B. gemäß FR-B-2 368 272) häufig auftreten. Die bei den Formen gemäß dieser französischen Patentschrift beobachteten Blutspiegelspitzen rühren davon her, daß Dipyridamol nur teilweise und individuell in verschieden hohem Maße resorbiert wird. Die Blutspiegelwerte fallen bei manchen Patienten nach kurzer Zeit unter den wirksamen Bereich ab bzw. werden zum Teil nicht erreicht (bei einem sogenannten "non-absorber"); die O-Acetylsalicylsäure erreicht dagegen bei jedem Patienten ihre pharmakologische Wirksamkeit.However, it is also possible, for example, to prepare dipyridamole granules, separating granules and acetylsalicylic acid granules separately and then compressing them into three-layer tablets; A pyrimidopyrimidine granulate can, however, also be filled into a capsule together with a coated tablet or film-coated tablet containing the O-acetylsalicylic acid. But if you put a special one If the pyrimidopyrimidine blood level is of a consistently high value, it is advantageous to start from pyrimidopyrimidine pellets, which enable a time-controlled and pH-controlled release of this active ingredient, and to process these together with the O-acetylsalicylic acid to give corresponding medicinal forms. It can also be advantageous here to produce compacts of O-acetylsalicylic acid with an appropriate covering through a film layer and to combine them with the pyrimidopyrimidine pellets. If it is desired to achieve a delayed release of O-acetylsalicylic acid, the pyrimidopyrimidine pellets can be coated with a layer which retards the release of this active ingredient and the cores containing O-acetylsalicylic acid with a layer soluble in gastric juice. In the case of dipyridamole pellets with a controlled release of the active ingredient, it is particularly advantageous to use those which have been prepared in accordance with the recipes described in DE-A-3 000 989.1. These pellets have a coating that acts as a dialysis membrane and releases the active ingredient dipyridamole in combination with acids in the gastrointestinal tract in a controlled manner. The structure and composition of the pellets leads to the release of dissolved dipyridamole in the form of its salts. Retard pellets produced in this way lead to complete absorption of the dipyridamole from the gastrointestinal tract. In this way, uniform blood levels can be achieved over 8 to 10 hours while avoiding blood level peaks, as frequently occur with the commercially available dipyridamole-acetylsalicylic acid forms (for example according to FR-B-2 368 272). The blood level peaks observed in the forms according to this French patent originate from the fact that dipyridamole is only partially and individually absorbed to different degrees. In some patients, the blood level values drop below the effective range after a short time or are sometimes not reached (with a so-called "non-absorber"); In contrast, O-acetylsalicylic acid achieves its pharmacological activity in every patient.
Ein bevorzugter Gegenstand der vorliegenden Erfindung betrifft also Arzneimittelformen, bestehend aus Dipyridamol und/oder Mopidamol in Verbindung mit einer physiologisch verträglichen Säure, wobei mindestens 1 Val Säure auf 1 Mol Dipyridamol oder Mopidamol kommen, umgeben von einer Umhüllung, die aus 50 bis 100% säureunlöslichen, darmsaftlöslichen Lacken und aus 50 bis 0% magen- und darmsaftunlöslichen Lacken besteht, wobei diese Komponente in Form von Granulaten oder Pellets vorliegt, und der Komponente O-Acetylsalicylsäure, die vorzugsweise mit einem magensaftlöslichen Überzug versehen ist und vorzugsweise als Dragée oder Filmtablette vorliegt, wobei die beiden Komponenten in einem Gewichtsverhältnis von mindestens 4,5 vorliegen müssen.A preferred subject of the present invention thus relates to pharmaceutical forms consisting of dipyridamole and / or mopidamol in combination with a physiologically acceptable acid, at least 1 val acid per 1 mol dipyridamole or mopidamol, surrounded by a covering which consists of 50 to 100% acid-insoluble , intestinal juice-soluble paints and consists of 50 to 0% gastric and intestinal juice-insoluble paints, this component being in the form of granules or pellets, and the component O-acetylsalicylic acid, which is preferably provided with a gastric juice-soluble coating and is preferably in the form of a tablet or film-coated tablet, the two components must be in a weight ratio of at least 4.5.
Während bevorzugte Formen gemäß der DE-Al-3 515 874 ein Gewichtsverhältnis von Pyrimido-pyrimidin zu O-Acetylsalicylsäure zwischen 0,6 und 1.5 besitzen (darüber hinausgehende Verhältnisse sind nicht durch Beispiele beschrieben), liegen diese Gewichtsverhältnisse im Falle der vorliegenden Erfindung über 4,5, vorzugsweise bei 8 bis 100.While preferred forms according to DE-Al-3 515 874 have a weight ratio of pyrimidopyrimidine to O-acetylsalicylic acid between 0.6 and 1.5 (further ratios are not described by examples), these weight ratios in the case of the present invention are above 4 , 5, preferably 8 to 100.
Hierbei enthalten die Arzneimittelformen zwischen 10 und 675 mg Dipyridamol und/oder Mopidamol und zwischen 1 und 150 mg O-Acetylsalicylsäure. Für Dipyridamol und Mopidamol bevorzugte Formen enthalten zwischen 75 und 400 mg dieses Wirkstoffes, ganz bevorzugte Formen zwischen 75 und 200 mg neben 5 bis 80 mg bzw. 5 bis 40 mg O-Acetylsalicylsäure. Im allgemeinen gibt man 2 bis 3 dieser Dosiseinheiten pro Tag, wobei je nach Schwere des Falles Abweichungen von dieser Dosierung nach oben und unten möglich sind. Die anzuwendende Dosierung hängt natürlich auch noch von anderen Faktoren ab, z. B. vom Alter, Gewicht, allgemeinen Gesundheitszustand des zu behandelnden Patienten, von der Schwere der Symptome bzw. der Erkrankung.The pharmaceutical forms contain between 10 and 675 mg dipyridamole and / or mopidamol and between 1 and 150 mg O-acetylsalicylic acid. Preferred forms for dipyridamole and mopidamole contain between 75 and 400 mg of this active ingredient, very preferred forms between 75 and 200 mg in addition to 5 to 80 mg and 5 to 40 mg of O-acetylsalicylic acid. In general, 2 to 3 of these dose units are given per day, depending on the severity of the case, deviations from this dose up and down are possible. The dosage to be used will of course also depend on other factors, e.g. B. from Age, weight, general state of health of the patient to be treated, the severity of the symptoms or the disease.
Die erfindungsgemäßen pharmazeutischen Zubereitungsformen enthalten gegebenenfalls noch sonstige übliche Träger- und/oder Hilfsstoffe und werden nach an sich üblichen Verfahren hergestellt. Als übliche Träger- und/oder Hilfsstoffe dienen z. B. Kartoffel-, Mais- oder Weizenstärke, Zellulose, Zellulosederivate, Siliziumdioxid, verschiedene Zucker, als Dragierstoffe Zucker und/oder Stärkesirup, Gelatine, Gummi arabicum, Polyvinylpyrrolidon, synthetische Zelluloseester, oberflächenaktive Substanzen, Weichmacher, und/oder Pigmente und ähnliche Zusatzstoffe, zur Herstellung von Tabletten und Kerne auch Schmiermittel, wie Magnesiumstearat.The pharmaceutical preparation forms according to the invention optionally also contain other customary excipients and / or auxiliaries and are prepared by processes which are customary per se. As usual carriers and / or auxiliaries z. B. potato, corn or wheat starch, cellulose, cellulose derivatives, silicon dioxide, various sugars, as sugar-coating agents sugar and / or starch syrup, gelatin, gum arabic, polyvinylpyrrolidone, synthetic cellulose esters, surface-active substances, plasticizers, and / or pigments and similar additives, for the production of tablets and cores also lubricants such as magnesium stearate.
Zur Herstellung eines erfindungsgemäßen Dipyridamol-Granulats werden z. B. Dipyridamol mit einer organischen Genußsäure, wie Fumarsäure, Weinsäure, Zitronensäure, Bernsteinsäure, Äpfelsäure und mit Bindern und/oder Haftmitteln, wie z. B. Polyvinylpyrrolidon, gemischt, mit einem Schmiermittel, wie z. B. Magnesiumstearat versetzt, das Gemisch anschließend verdichtet, z. B. mit Hilfe eines Walzenkompaktors, und zu Granulaten aufgebrochen, z. B. unter Verwendung eines Trockengranuliergerätes mit nachgeschalteter Siebeinrichtung.To produce a dipyridamole granulate according to the invention, for. B. dipyridamole with an organic edible acid, such as fumaric acid, tartaric acid, citric acid, succinic acid, malic acid and with binders and / or adhesives, such as. B. polyvinylpyrrolidone, mixed with a lubricant such as. B. magnesium stearate, the mixture is subsequently compressed, for. B. with the help of a roller compactor, and broken up into granules, for. B. using a dry pelletizer with a downstream screening device.
Die Herstellung von Dipyridamol-Pellets geschieht vorzugsweise unter Verwendung von Starterkernen, die vorteilhafterweise aus einer organischen Genußsäure, z. B. aus ausgerundeten Weinsäurekristallen, bestehen (Durchmesser der Starterkerne 0,5 bis 0,9 mm), auf welche in einem Kessel eine Suspension aus Dipyridamol in einem Alkohol oder Alkohol/Wasser-Gemisch und aus einem Binder, wie z. B. Polyvinylpyrrolidon, so lange aufgesprüht wird, bis die entstehenden Wirkstoffpellets die vorgeschriebene Menge Dipyridamol enthalten (die Pellets weisen dann einen Durchmesser zwischen 0,9 und 1,5 mm auf). Diese Pellets werden, sofern man eine retardierte Wirkstoff-Abgabe beabsichtigt, mit einem Lack überzogen, der zu 50 bis 100% aus säureunlöslichen, darmsaftlöslichen Lacken und zu 50 bis 0% aus magen- und darmsaftunlöslichen Lacken besteht. Bewährt hat sich ein Lack aus Methacrylsäure-/Methacrylsäureester-Copolymeren (Eudragit S®) und Hydroxypropylmethylcellulosephthalat (HP 55®), dem noch Weichmacher und Füllstoffe, z. B. Talkum beigefügt sein können. Als darmsaftlösliche Lackkomponenten kommen auch noch Celluloseacetatphthalat, Ethylcel lulosephthalat, Hydroxypropylmethylcellulosesuccinat, Celluloseacetatsuccinat, Hydroxypropylmethylcellulosehexahydrophthalat, Celluloseacetathexahydrophthalat, Hydroxypropylmethylcellulosetrimellitat, Methacrylsäure-Methacrylsäureester-Mischpolymerisat (Säurezahl 300 bis 330, Eudragit L®) oder Gemische dieser Stoffe in Frage. Darmsaft- und Magensaftunlösliche Lacke als Beimischungen können sein: Lacke auf Acrylat- bzw. Methacrylatbasis (Eudragit retard S® und Eudragit retard L®), auch in Verbindung von bis zu 14 Gew.-% Ethylcellulose.Dipyridamole pellets are preferably produced using starter cores, which are advantageously made from an organic edible acid, e.g. B. from rounded tartaric acid crystals exist (diameter of the starter cores 0.5 to 0.9 mm), on which in a kettle a suspension of dipyridamole in an alcohol or alcohol / water mixture and from a binder, such as. B. polyvinylpyrrolidone is sprayed on until the resulting active substance pellets contain the prescribed amount of dipyridamole (the pellets then have a diameter between 0.9 and 1.5 mm). These pellets, provided you have one Delayed release of active ingredient is intended to be coated with a varnish which consists of 50 to 100% acid-insoluble, intestinal juice-soluble varnishes and 50 to 0% of gastric and intestinal juice-insoluble varnishes. A varnish made of methacrylic acid / methacrylic acid ester copolymers (Eudragit S®) and hydroxypropylmethyl cellulose phthalate (HP 55®), which contains plasticizers and fillers, e.g. B. talc can be added. As intestinal juice-soluble coating components are also cellulose acetate phthalate, lulosephthalat Ethylcel, hydroxypropylmethylcellulose succinate, cellulose acetate succinate, hydroxypropylmethyl cellulose, cellulose acetate hexahydrophthalate, hydroxypropylmethyl cellulose trimellitate, methacrylic acid-methacrylic acid copolymer (acid number 300 to 330, Eudragit L®), or mixtures of these substances in question. Intestinal juice and gastric juice-insoluble varnishes as admixtures can be: varnishes based on acrylate or methacrylate (Eudragit retard S® and Eudragit retard L®), also in combination with up to 14% by weight of ethyl cellulose.
Dipyridamol (und/oder Mopidamol) -Pellets lassen sich aber auch dadurch erhalten, daß man in einen Extruder (z. B. Doppelschneckenextruder) ein Pulvergemisch aus Dipyridamol (und/oder Mopidamol) und der berechneten Menge einer organischen Genußsäure (z. B. Fumarsäure) und Binder und gegebenenfalls sonstige Hilfsmittel einführt, hierzu noch ein organisches Lösungsmittel zudosiert und die Masse durchmischt. Die befeuchtete Masse wird in Form von Spaghettis ausgedrückt, die auf einer schnell drehenden Platte zu hochverdichteten Pellets gerundet werden. Die Pellets werden anschließend getrccknet und, gegebenenfalls, mit einem wie oben beschriebenen retardierenden Lack überzogen.Dipyridamole (and / or mopidamole) pellets can also be obtained by placing a powder mixture of dipyridamole (and / or mopidamole) and the calculated amount of an organic edible acid (e.g. in an extruder (e.g. twin screw extruder)). Fumaric acid) and binder and possibly other auxiliaries, an organic solvent is added and the mixture is mixed. The moistened mass is expressed in the form of spaghetti, which are rounded on a fast rotating plate to high-density pellets. The pellets are then dried and, if appropriate, coated with a retarding lacquer as described above.
Die O-Acetylsalicylsäure kann einmal in Form von gepreßten Kernen, die mit einer isolierenden Deckschicht überzogen sind, oder in Form von Filmtabletten eingesetzt werden. Die Formlinge werden aus der O-Acetylsalicylsäure, Fließ- und Gleitmitteln und Träger- und/oder Verdünnungsmitteln, wie z. B. fließfähige Laktose, mikrokristalline Cellulose, getrocknete Maisstärke, Aluminium- oder Magnesiumstearat, in an sich bekannter Weise durch Herstellung und Verpreßung eines entsprechenden Granulats gewonnen. Die Kerne überzieht man, gegebenenfalls in mehreren Schritten, mit einer Dragiersuspension, die z. B. aus Zuckern (wie Saccharose), Gummi arabicum, Talk und ähnlichen Stoffen besteht.O-acetylsalicylic acid can be used once in the form of pressed cores, which are covered with an insulating cover layer, or in the form of film-coated tablets. The moldings are made from O-acetylsalicylic acid, flow and Lubricants and carriers and / or diluents, such as. B. flowable lactose, microcrystalline cellulose, dried corn starch, aluminum or magnesium stearate, obtained in a manner known per se by producing and pressing a corresponding granulate. The cores are coated, if necessary in several steps, with a coating suspension which, for. B. from sugars (such as sucrose), gum arabic, talc and similar substances.
Eine typische Drei-Schicht-Tablette wird beispielsweise dadurch gewonnen, daß ein Pyrimidopyrimidingranulat, ein O-Acetylsalicylsäure-Granulat und ein Trenngranulat, das z. B. aus Lactose, mikrokristalliner Zellulose und Polyvinylpyrrolidon aufgebaut ist und ein Gleitmittel enthält, mittels einer speziellen Tablettenpresse mit 3 Fülltrichtern und 3 Preßstationen so verpreßt wird, daß die neutrale Trennschicht zwischen den beiden gepreßten Wirkstoffen liegt.A typical three-layer tablet is obtained, for example, by adding a pyrimidopyrimidine granulate, an O-acetylsalicylic acid granulate and a separating granulate which, for. B. is made of lactose, microcrystalline cellulose and polyvinylpyrrolidone and contains a lubricant, is pressed by means of a special tablet press with 3 filling funnels and 3 pressing stations so that the neutral separating layer lies between the two pressed active ingredients.
Die erfindungsgemäße Kombination wird als ein antithrombotisches, die Blutplättchenaggregation und die Metastasenwirkung inhibierendes Mittel bei Menschen und Tieren angewandt; die Kombination verhindert die Bildung und Aufrechterhaltung von venösen und arteriellen Blutgerinnseln, sie verhindert somit vorübergehende ischämische Anfälle und dient der vorbeugenden Beeinflussung zur Vermeidung von Herzinfarkten und Schlaganfällen. Sie ist gut geeignet zur Verhinderung der Bildung und Aufrechterhaltung eines Thrombus bei vorliegenden Arteriosklerosen oder nach operativen Eingriffen oder sonstigen mit Thromboseneigung einhergehenden Zuständen; bei der Anwendung kommen aber auch die typischen Eigenschaften der Einzelkomponenten zur Wirkung, z. B. kommt es zu einer verbesserten O₂-Versorgung des Herzmuskels und zur Hemmung entzündlicher Vorgänge, desweiteren zu einer Schmerzlinderung.The combination according to the invention is used as an antithrombotic agent which inhibits blood platelet aggregation and the effect of metastases in humans and animals; the combination prevents the formation and maintenance of venous and arterial blood clots, it thus prevents transient ischemic attacks and serves as a preventive measure to prevent heart attacks and strokes. It is well-suited for preventing the formation and maintenance of a thrombus in the presence of arteriosclerosis or after surgery or other conditions associated with thrombosis; in use, however, the typical properties of the individual components also come into effect, e.g. B. there is an improved O₂ supply to the heart muscle and inhibition of inflammatory processes, furthermore to pain relief.
Die Untersuchung der antithrombotischen Wirkung bei erfindungsgemäßer gleichzeitiger oraler Gabe von 5 mg/kg Dipyridamol und 0,05 mg/kg O-Acetylsalicylsäure (Gewichtsverhältnis Dipyridamol zu O-Acetylsalicylsäure = 100) und, vergleichend hierzu, bei einer (gemäß der Europäischen Anmeldung Nr. 85 108 761.9) zeitlich versetzt verabreichten oralen Gabe von 5 mg/kg Dipyridamol und 5 mg/kg O-Acetylsalicylsäure an Ratten (FW 49) mit einem Körpergewicht von 60 bis 80 g vor Beginn der Untersuchung, erfolgte durch das Setzen eines Reizes zur Thrombusbildung an Gefäßen des Mesenteriums und durch die Beobachtung des zeitlichen Verhaltens der Größe dieser Thromben. Es wurden jeweils Gruppen von 5 Tieren verwendet. Ein standardisierter Reiz führt zu einem Thrombus mit einer Größe, die 80% des Gefäßdurchmessers verschließt. Zwischen der gleichzeitigen oralen Gabe der Substanzen gemäß vorliegender Erfindung und der Setzung des Thrombus bzw. der eigentlichen Durchführung der Messungen wird ein Intervall von einer Stunde gewählt. Die zeitlich versetzte orale Gabe der Substanzen gemäß der obengennanten europäischen Anmeldung erfolgte so, daß zuerst Dipyridamol 90 Minuten vor der Gabe der O-Acetylsalicylsäure, letztere 60 Minuten vor dem Setzen des Thrombus und den beginnenden Messungen erfolgte; mit anderen Worten, Dipyridamol wurde 150 Minuten, O-Acetylsalicylsäure 60 Minuten vor Versuchsbeginn gegeben.The investigation of the antithrombotic effect with simultaneous oral administration according to the invention of 5 mg / kg dipyridamole and 0.05 mg / kg O-acetylsalicylic acid (weight ratio dipyridamole to O-acetylsalicylic acid = 100) and, in comparison, with one (according to European Application No. 85 108 761.9) Oral administration of 5 mg / kg of dipyridamole and 5 mg / kg of O-acetylsalicylic acid to rats (FW 49) with a body weight of 60 to 80 g prior to the start of the study was carried out at different times by setting a stimulus to form a thrombus on vessels of the mesentery and by observing the temporal behavior of the size of these thrombi. Groups of 5 animals were used in each case. A standardized stimulus leads to a thrombus with a size that closes 80% of the vessel diameter. An interval of one hour is chosen between the simultaneous oral administration of the substances according to the present invention and the setting of the thrombus or the actual implementation of the measurements. The staggered oral administration of the substances according to the above-mentioned European application was such that dipyridamole was first given 90 minutes before the administration of O-acetylsalicylic acid, the latter 60 minutes before the thrombus was set and the measurements began; in other words, dipyridamole was given 150 minutes and O-
Zur Durchführung des Versuches wurden die Tiere mit ca. 60 mg/kg Nembutal i.p. narkotisiert, ihr Abdomen eröffnet und ein Teil des Mesenteriums nach außen luxiert und mit physiologischer, erwärmter Nährlösung während des Ablaufs der Messungen überspült.To carry out the experiment, the animals were given approximately 60 mg / kg of Nembutal i.p. anesthetized, her abdomen opened and part of the mesentery dislodged to the outside and washed over with physiological, heated nutrient solution during the course of the measurements.
Unter intravitalmikroskopischer Beobachtung wurde eine Platinelektrode auf eine äußere Gefäßwand des Mesenteriums gesetzt. Eine Gegenelektrode wurde unter das Mesenterium geschoben. Eine fest gewählte Kombination zwischen angelegter Gleichspannung (150 V) und Strom (1,5 mA) in einem Impuls mit vorgegebener Länge (100 ms) führt bei einer Venole von ca. 300 µm Durchmesser zu einer reproduzierbaren Bildung eines Thrombus, der in aller Regel 80% des Gefäßdurchmessers verschließt. Die Größe des Thrombus wird im Abstand von 10 Sekunden, später von 30 Sekunden in einem Zeitbereich bis zu 20 Minuten nach Reizung des Gefäßes gemessen und als Thrombusgröße (senkrecht zur Gefäßwand) in Prozent des Gefäßinnendurchmessers angegeben.A platinum electrode was placed on an outer vessel wall of the mesentery under intravital microscopic observation. A counter electrode was inserted under the mesentery. A fixed combination between created DC voltage (150 V) and current (1.5 mA) in one pulse with a predetermined length (100 ms) leads to a reproducible formation of a thrombus in a venule of approx. 300 µm diameter, which usually closes 80% of the vessel diameter. The size of the thrombus is measured at intervals of 10 seconds, later 30 seconds in a time range up to 20 minutes after irritation of the vessel, and is given as the thrombus size (perpendicular to the vessel wall) as a percentage of the inner diameter of the vessel.
Innerhalb des Beobachtungsintervalles von 20 Minuten ist bei dem jeweiligen Kontrollkollektiv, das aus nur mit dem jeweiligen Lösungs- bzw. Trägermittel oral behandelten Tieren besteht, eine stabile Thrombusgröße von ca. 85% zu beobachten (vgl. Abbildung 7, N=68 Kontrollmessungen; Mittelwerte zu jedem Zeitpunkt mit Angabe der Standardabweichung [± SD]).Within the observation interval of 20 minutes, a stable thrombus size of approx. 85% can be observed in the respective control group, which consists of animals orally treated only with the respective solvent or carrier agent (see Figure 7, N = 68 control measurements; mean values at any time with indication of the standard deviation [± SD]).
Für akut auftretende Gefäßverschlüsse, wie z. B. bei einem Herzinfarkt oder bei einem Schlaganfall, wird allgemein ein rasch gebildeter Thrombus an einer bestehenden Verletzung oder krankhaften Veränderung der Gefäßwand verantwortlich gemacht. Bei einer die Thrombusbildung hemmenden Medikation ist zu erwarten, daß der entstehende Thrombus die in der Kontrollgruppe erreichte Größe von 85% des Gefäßdurchmessers nicht erreicht. Nur so kann verhindert werden, daß es durch die ungehemmte Bildung eines Thrombus zu einer Verlegung des Blutflusses kommt, was üblicherweise schwer wiegende Folgen durch die dann entstehenden ischämischen Schäden nach sich zieht (z. B. Herzinfarkt, Schlaganfall). Eine Medikation mit einer Substanz oder Substanzkombination, die nur eine schnelle Auflösung eines Thrombus zur Folge hat, wird im allgemeinen die Bildung des Thrombus bis zu einer mit der Kontrollgruppe vergleichbaren Größe zulassen, um diesen jedoch in dem nachfolgenden Untersuchungszeitraum deutlich zu verringern, d.h. eine initiale Verlegung des Blutflusses wird somit nicht verhindert. Die Abbildungen 1 und 2 zeigen den zeitlichen Verlauf der Thrombusgröße nach elektrischer Thrombussetzung für eine Kombination gemäß der oben angegebenen Europäischen Patentanmeldung Nr. 85 108 761.9 (Abbildung 1) und eine erfindungsgemäße Kombination (Abbildung 2).For acute vascular occlusions, such as B. in a heart attack or a stroke, a rapidly formed thrombus is generally held responsible for an existing injury or pathological change in the vessel wall. In the case of medication which inhibits thrombus formation, it is to be expected that the thrombus formed will not reach the size of 85% of the vessel diameter achieved in the control group. This is the only way to prevent the uninhibited formation of a thrombus from obstructing blood flow, which usually has serious consequences from the ischemic damage that then arises (e.g. heart attack, stroke). Medication with a substance or combination of substances that only results in a rapid dissolution of a thrombus will generally allow the formation of the thrombus to a size comparable to that of the control group, but to reduce it significantly in the subsequent investigation period, ie an initial one This does not prevent blood flow from being blocked. Figures 1 and 2 show the time course of the thrombus size according to electrical Thrombus setting for a combination according to the above-mentioned European patent application No. 85 108 761.9 (Figure 1) and a combination according to the invention (Figure 2).
Die Abbildung 1 zeigt den Verlauf der Thrombusgröße innerhalb von 20 Minuten nach Setzen des Thrombus nach einer oralen Gabe von 5 mg/kg O-Acetylsalicylsäure 60 Minuten vor Durchführung der Messung und einer oralen Gabe von 5 mg/kg Dipyridamol 150 Minuten vor Durchführung der Messung. Bei der Kontrollgruppe bleibt dabei die Größe des Thrombus während der ersten Hälfte des Beobachtungszeitraumes bei ca. 85%, um in der zweiten Hälfte geringfügig abzufallen, während in der behandelten Gruppe die Größe des Thrombus zunächst innerhalb der ersten 30 Sekunden Werte nahe derjenigen des Kontrollversuchs annimmt, um im weiteren Versuchsverlauf jedoch sich stärker zu verringern.Figure 1 shows the course of the thrombus size within 20 minutes after setting the thrombus after an oral administration of 5 mg / kg O-
Ein deutlich unterschiedlicher Zeitverlauf zeigt sich in Abbildung 2. Darin ist eine Kontrollgruppe mit einer Gruppe verglichen worden, die erfindungsgemäß gleichzeitig oral 5 mg/kg Dipyridamol und 0,05 mg/kg O-Acetylsalicylsäure 60 Minuten vor dem Beginn der Messungen erhalten hat. Im Gegensatz zu der Abbildung 1 zeigt die behandelte Gruppe bereits zu Beginn und im ersten Zeitabschnitt des Versuches eine deutlich gehemmte Bildung des Thrombus, die bereits zu Beginn des Versuchs die Werte annimmt, die im Falle der behandelten Gruppe der Abbildung 1 erst im zweiten Drittel des Versuches erreicht wird.A clearly different time course is shown in Figure 2. A control group was compared with a group that according to the invention received 5 mg / kg of dipyridamole orally and 0.05 mg / kg of O-acetylsalicylic acid simultaneously 60 minutes before the start of the measurements. In contrast to Figure 1, the treated group showed a clearly inhibited formation of the thrombus at the beginning and in the first period of the experiment, which at the beginning of the experiment assumed the values that in the case of the treated group of Figure 1 only in the second third of the Attempt is achieved.
Aus diesen Zeitverläufen der Abbildungen 1 und 2 wird erkennbar, daß die der Abbildung 2 zugrundegelegte Vorbehandlung bereits die Entstehung des Thrombus verhinderte, während die der Abbildung 1 zugrundeliegende Behandlung lediglich eine beschleunigte Auflösung des gesetzten Thrombus bewirkte, die aber auch bei der Behandlung, die der Abbildung 2 zugrunde liegt, in gleichem Maße zu beobachten ist.From these time profiles of Figures 1 and 2 it can be seen that the pretreatment on which Figure 2 was based already prevented the development of the thrombus, while the treatment on which Figure 1 was based only brought about an accelerated dissolution of the thrombus set, but also in the treatment which the Figure 2 is based, can be observed to the same extent.
In den Abbildungen 3 bis 6 werden die prozentualen Thrombusgrößen in einzelnen Zeitabschnitten zusammengefaßt und jeweils einander gegenübergestellt. Die Kolonnen A repräsentieren die Thrombusgrößen der Kontrollgruppe, d.h. die Thrombusgröße der Kontrollgruppe ist auf 100% gesetzt worden. Die Kolonnen B zeigen die Thrombusgrößen einer Kombination von 5 mg/kg Dipyridamol und 5 mg/kg O-Acetylsalicylsäure entsprechend der Kurve in Abbildung 1, die Kolonnen C die Thrombusgrößen bei vorheriger Applikation von 2,5 mg/kg O-Acetylsalicylsäure, die Kolonnen D bei vorheriger Applikation von 5 mg/kg Dipyridamol und die Kolonnen E nach vorheriger Applikation der erfindungsgemäßen Kombination von 5 mg/kg Dipyridamol und 0,05 mg/kg O-Acetylsalicylsäure entsprechend der Kurve in Abbildung 2, die Kolonnen F von 2 mg/kg Dipyridamol und 0,05 mg/kg O-Acetylsalicylsäure (alle Applikationen erfolgten oral).Figures 3 to 6 summarize the percentage thrombus sizes in individual time periods and compare them with each other. Columns A represent the thrombus sizes of the control group, i.e. the control group thrombus size was set to 100%. Columns B show the thrombus sizes of a combination of 5 mg / kg dipyridamole and 5 mg / kg O-acetylsalicylic acid according to the curve in Figure 1, columns C show the thrombus sizes after prior application of 2.5 mg / kg O-acetylsalicylic acid, the columns D with prior application of 5 mg / kg dipyridamole and the columns E after prior application of the combination according to the invention of 5 mg / kg dipyridamole and 0.05 mg / kg O-acetylsalicylic acid according to the curve in Figure 2, the columns F of 2 mg / kg of dipyridamole and 0.05 mg / kg of O-acetylsalicylic acid (all applications were oral).
Die Abbildung 3 gibt die prozentuale Reduktion des 85%igen Verschlußes in der Zeit von 10 Sekunden bis 1 Minute nach der Reizung des Gefäßes wieder, verglichen mit den Kontrollen, die mit 100% eingesetzt sind. Wie man hieraus sieht, ist bei Vorhandensein der erfindungsgemäßen Kombination (Kolonne E) die Größe des bei der elektrischen Reizung gesetzten Thrombus bereits um ca. 20% (also praktisch schon in statu nascendi) verringert; nach der Verabreichung der vorbekannten Kombination (Kolonne B) dagegen nur um ca. 5%; dies bedeutet, daß bei Verabreichung der erfindungsgemäßen Kombination die Thrombusbildung bereits deutlich gehindert wird.Figure 3 shows the percentage reduction in the 85% occlusion from 10 seconds to 1 minute after irritation of the vessel compared to the controls used at 100%. As can be seen from this, when the combination according to the invention (column E) is present, the size of the thrombus set during the electrical stimulation is already reduced by approximately 20% (practically already in statu nascendi); after administration of the previously known combination (column B), however, only by about 5%; this means that the thrombus formation is already significantly prevented when the combination according to the invention is administered.
Die Abbildung 4 zeigt die gleichen Verhältnisse im Zeitbereich 2 bis 4 Minuten ab der Reizung. Die Thrombusgröße nimmt allgemein ab, am stärksten ausgeprägt ist die Reduktion bei der erfindungsgemäßen Kombination.Figure 4 shows the same conditions in the
Die Abbildung 5 gibt die Verhältnisse im Zeitbereich 5 bis 10 Minuten nach Reizung, die Abbildung 6 den Zeitbereich 10 bis 20 Minuten wieder. Erst nach ca. 15 Minuten wird auch bei der vorbekannten Kombination eine Reduktion der Thrombusgröße erreicht, welche der durch die erfindungsgemäße Kombination erzielten entspricht. Die O-Acetylsalicylsäure und das Dipyridamol allein bewirken keine signifikante Verminderung der Thrombusgröße. Vergleicht man besonders in Abbildung 6 die prozentualen Senkungen miteinander, so sieht man, daß es sich bei den Acetylsalicylsäure-Dipyridamol-Kombinationen um überadditive bzw. synergistische Effekte handelt. Aus der Abbildung 3 wird aber noch ein weiterer Zusammenhang sichtbar: bei Erhöhung der O-Actylsalicylsäuredosis gegenüber der Dipyridamoldosis nimmt der hemmende Effekt auf die Thrombusbildung ab; es hat sich gezeigt, daß bei Kombinationen mit Gewichtsverhältnissen von Dipyridamol zu O-Acetylsalicylsäure von kleiner als 4 sehr schnell Verhältnisse erzielt werden, die der in der Abbildung 1 gezeigten Kurve bzw. den in den Abbildungen 3 bis 6 durch die Kolonnen B gezeigten Werten entsprechen. Dadurch wird aber auch klar ersichtlich, daß die erfindungsgemäßen Kombinationen den vorbekannten Kombinationen bei der Thrombusverhütung deutlich überlegen sind. Dabei sollte nicht unerwähnt bleiben, daß dieser Effekt mit einer Kombination erreicht wird, in der der O-Acetylsalicylsäureanteil sehr gering ist, so daß die Nebenwirkungen dieser Substanz nicht zu erwarten sind.Figure 5 shows the conditions in the
Dafür, daß nicht nur die Applikationsfolge von Dipyridamol und Acetylsalicylsäure sondern bei gleichzeitiger Applikation auch die Dosisrelation dieser beiden Wirkstoffe von entscheidender Bedeutung für die Verhinderung von Gefäßverschlüssen durch Thromben ist, zeigten Versuche am Modell der rekurrierenden Thrombose an der Kaninchenaorta. In Anlehnung an das von Folts, JD, in Circulation 54 (1976), Seite 365, beschriebene Modell an der Arteria circumflexa des Hundes wurde ein rekurrierendes Modell an der abdominalen Aorta des Kaninchens entwickelt. Nach Anaesthesie mit Rompun, initial mit 10 mg/kg Rompun und 70 mg/kg Ketanest i.m. und, kontinuierlich, mit 4 mg/kg/h Rompun und 20 mg/kg/h Ketanest i.m. während der Dauer des Versuches (Dauerinfusion), wurden Kaninchen (New Zealand Whites von ca. 3 kg Körpergewicht) durch Sagitalschnitt laparotomiert. Die abdominale Aorta wurde distal von der Arteria renalis freigelegt; es wurde eine elektromagnetische Flow-Sonde (alternativ eignet sich hierzu auch eine Ultraschall-Flow-Sonde) am proximalen Ende dieses Abschnittes angebracht. Distal zu der Flow-Sonde wurde die Aorta mechanisch durch wiederholtes Quetschen mittels einer Arterienklemme (eines Hemostats) geschädigt. Diese Prozedur führte zu einer Gefäßschädigung durch Ruptur der Lumenauskleidung, Freilegung subendothelialer Strukturen, Bindegewebe und glatter Muskeln. Am Orte der Gefäßschädigung wird eine mechanische Stenose angebracht, die den Fluß durch die Aorta auf ungefähr 40 % des Ausgangswertes reduziert.Experiments with the model of recurrent thrombosis in the rabbit aorta have shown that not only the application sequence of dipyridamole and acetylsalicylic acid, but also the dose ratio of these two active ingredients is of crucial importance for the prevention of vascular occlusion by thrombi when used simultaneously. Following the model of the dog's circumflex artery described by Folts, JD, Circulation 54 (1976), page 365, a recurrent model of the abdominal aorta of the Rabbit developed. After anesthesia with Rompun, initially with 10 mg / kg Rompun and 70 mg / kg Ketanest in and, continuously, with 4 mg / kg / h Rompun and 20 mg / kg / h Ketanest during the duration of the experiment (continuous infusion) Rabbits (New Zealand Whites of approx. 3 kg body weight) laparotomized by sagital incision. The abdominal aorta was exposed distally from the renal artery; an electromagnetic flow probe (alternatively an ultrasonic flow probe is also suitable) was attached to the proximal end of this section. Distal to the flow probe, the aorta was mechanically damaged by repeated squeezing using an artery clamp (a hemostat). This procedure resulted in vascular damage from rupture of the lumen lining, exposure of subendothelial structures, connective tissue and smooth muscles. A mechanical stenosis is placed at the site of the vascular damage, reducing the flow through the aorta to approximately 40% of the initial value.
Nach dieser Schädigung beobachtet man, daß der totale Volumenfluß durch die Aorta im Verlauf von einigen Minuten stetig reduziert wird bis zum vollständigen Sistieren des Flusses. Das Gefäß bleibt verschlossen, bis der gebildete Thrombus in dem verengten Segment durch mechanische Agitation losgelöst, d. h. embolisiert wird. Dadurch wird der ursprüngliche Fluß wieder hergestellt. Danach folgt wiederum eine graduelle Abnahme des Blutflusses bis zum erneuten Stillstand. Nach erneuter mechanischer Agitation bzw. Embolisierung des Thrombus läßt sich dieser rekurrierende Prozeß immer und immer wieder verfolgen.After this damage, it is observed that the total volume flow through the aorta is steadily reduced over the course of a few minutes until the flow has completely stopped. The vessel remains closed until the thrombus formed in the narrowed segment is detached by mechanical agitation, i.e. H. is embolized. This will restore the original river. This is followed by a gradual decrease in blood flow until it stops again. After repeated mechanical agitation or embolization of the thrombus, this recurrent process can be followed again and again.
Zu Beginn eines jeden Versuchs wird eine Anzahl von Flow-Reduktions-Cyclen über eine Periode von 30 Minuten zu Kontrollzwecken festgehalten. Darauf wird der zu prüfende Wirkstoff verabreicht, entweder intravenös oder in die Mesenterialvene. Über eine Periode von 30 bis 60 Minuten sowie über eine weitere Periode von 60 bis 90 Minuten nach der Applikation des Wirkstoffes werden die beobachteten Flow-Reduktions-Cyclen festgehalten. Ein wirksamer Stoff verzögert das Versiegen des Blutflusses, embolisiert spontan den sich bildenden Thrombus in dem stenosierten Segment oder stellt - bei guter Wirkung - den ursprünglichen Fluß des Blutes ohne periodische Reduktion wieder her. Der maximal erreichbare antithrombotische Effekt entspricht also der vollständigen Wiederherstellung des durch die Stenose möglichen maximalen Blutflusses (100 % "free Flow").At the beginning of each experiment, a number of flow reduction cycles are recorded over a period of 30 minutes for control purposes. The active substance to be tested is then administered, either intravenously or into the mesenteric vein. Over a period of 30 to 60 minutes as well as over a further period of 60 to 90 minutes after the application of the active ingredient, the observed flow reduction cycles are recorded. An active substance delays the drying up of the blood flow, spontaneously embolizes the thrombus that forms in the stenosed segment or - if it works - restores the original flow of the blood without periodic reduction. The maximum achievable antithrombotic effect corresponds to the complete restoration of the maximum blood flow possible through the stenosis (100% "free flow").
Für die numerische Auswertung der Ergebnisse wird das Muster der Flow-Reduktions-Zyclen vor Gabe des Wirkstoffes zu Vergleichszwecken ermittelt. Aus dem Unterschied in der Flow-Reduktions-Rate und der Amplitude der zyklischen Flow-Oscilation wird mit einem Computer ein Flow-Muster konstruiert, das die Zunahme des freien Flusses zu jedem Zeitpunkt nach der Wirkstoffgabe wiedergibt. Mechanisch herbeigeführte Thrombus-Embolisierungen werden negativ veranschlagt im Vergleich zu spontanen Thrombus-Embolisierungen (d. h. es erfolgt keine oder, gegebenenfalls eine positive Korrektur). Aus diesen korrigierten Kurven errechnet der Computer den Parameter "Freier Fluß" ("free Flow") für 20 oder 30 minütige Intervalle vor und nach der Wirkstoffgabe. Um topische Effekte, die bei oraler Gabe der Acetylsalicylsäure auftreten können, zu minimieren, wurden die Wirkstoffe als Bolus in die Mesenterialvene verabreicht.For the numerical evaluation of the results, the pattern of the flow reduction cycles is determined before administration of the active ingredient for comparison purposes. From the difference in the flow reduction rate and the amplitude of the cyclic flow oscillation, a flow pattern is constructed with a computer, which reflects the increase in free flow at any time after the active substance has been administered. Mechanically induced thrombus embolizations are negatively assessed compared to spontaneous thrombus embolizations (i.e. there is no or, if necessary, a positive correction). From these corrected curves, the computer calculates the parameter "free flow" for 20 or 30 minute intervals before and after the administration of the active ingredient. In order to minimize topical effects, which can occur with oral administration of acetylsalicylic acid, the active substances were administered as a bolus in the mesenteric vein.
100 %iger freier Flow bedeutet einen ungehemmten Fluß durch die Aorta ohne Hemmung durch Thromben (jedoch mit besagter mechanischer Einengung). Es wurden jeweils vier Tiere bei jeder Gruppe verwendet. Es wurden folgende Dosen bzw. Dosis-Kombinationen angewandt:
- 1.)
Dipyridamol 5 mg/kg - 2.) Acetylsalicylsäure 50 µg/kg
- 3.)
Acetylsalicylsäure 100 µg/kg - 4.)
Acetylsalicylsäure 1 mg/kg - 5.) Acetylsalicylsäure 500 µg/kg
- 6.) Acetylsalicylsäure+Dipyridamol 500 µg/kg+5 mg/kg (Abb.8)
- 7.)
Acetylsalicylsäure+Dipyridamol 50 µg/kg+5 mg/kg (Abb.9) - 8.)
Acetylsalicylsäure+Dipyridamol 100 µg/kg+5 mg/kg (Abb.10) - 9.)
Acetylsalicylsäure+Dipyridamol 5 mg/kg+1 mg/kg (Abb.11)
- 1.) Dipyridamole 5 mg / kg
- 2.)
Acetylsalicylic acid 50 µg / kg - 3.)
Acetylsalicylic acid 100 µg / kg - 4.)
Acetylsalicylic acid 1 mg / kg - 5.) Acetylsalicylic acid 500 µg / kg
- 6.) Acetylsalicylic acid + dipyridamole 500 µg / kg + 5 mg / kg (Fig.8)
- 7.) Acetylsalicylic acid +
dipyridamole 50 µg / kg + 5 mg / kg (Fig.9) - 8.) Acetylsalicylic acid +
dipyridamole 100 µg / kg + 5 mg / kg (Fig.10) - 9.) acetylsalicylic acid +
dipyridamole 5 mg / kg + 1 mg / kg (Fig.11)
Die ersten fünf Einzelsubstanz-Behandlungen zeigten überhaupt keine Wirkungen in diesem Modell. Kombinationen von Dipyridamol mit Acetylsalicylsäure, die simultan gegeben wurden, zeigten dagegen eine Zunahme des freien Flußes mit zunehmender Zeit. Hierzu wird auf die Abbildungen 8 bis 10 verwiesen. Aus diesen Figuren wird ersichtlich, daß das Verhältnis von Dipyridamol zu Acetylsalicylsäure von 10:1 weniger wirksam ist als das von 100:1, letzteres ist aber wiederum weniger wirksam als das von 50:1, was die Zunahme des freien Flusses betrifft.The first five individual substance treatments showed no effects at all in this model. Combinations of dipyridamole with acetylsalicylic acid, which were given simultaneously, showed an increase in free flow with increasing time. Please refer to Figures 8 to 10. It can be seen from these figures that the ratio of dipyridamole to acetylsalicylic acid of 10: 1 is less effective than that of 100: 1, but the latter is again less effective than that of 50: 1 in terms of increasing free flow.
Die Abbildung 11 gibt in etwa die Verhältnisse bei einer bekannten Kombination (Asasantin®) wieder; es wird ersichtlich, daß diese deutlich weniger wirksam ist als die erfindungsgemäßen Kombinationen. Da bei den bisherigen bekannten Kombinationen stets vergleichsweise hohe Konzentrationen an Acetylsalicylsäure verwendet werden, ist auch bisher auf ein erhöhtes Blutungsrisiko wiederholt hingewiesen worden. Die erfindungsgemäßen Kombinationen zeigen überraschenderweise eine deutlich bessere Wirkung bei einer wesentlich verringerten Konzentration von Acetylsalicylsäure, was eine sehr deutliche Verringerung bzw. sogar Vermeidung des Blutungsrisikos bedeutet.Figure 11 shows roughly the conditions for a known combination (Asasantin®); it can be seen that this is significantly less effective than the combinations according to the invention. Since comparatively high concentrations of acetylsalicylic acid are always used in the previously known combinations, an increased risk of bleeding has also been repeatedly pointed out. The combinations according to the invention surprisingly show a significantly better effect with a significantly reduced concentration of acetylsalicylic acid, which means a very significant reduction or even avoidance of the risk of bleeding.
Eine Kombination der beiden Wirkstoffe interveniert bereits im ersten Stadium der Thrombus-Bildung; die Gefahr einer rekurrierenden Thrombosis in einem System mit hohem Druck und hohen Fluß- und Scherraten ("high flow/high pressure" - System) wird signifikant vermindert. Die bevorzugte Dosis liegt (beim Kaninchen) bei 50:1 (Dipyridamol zu Acetylsalicylsäure). Man sollte aber nicht außer Acht lassen, daß Kaninchen im allgemeinen weniger sensitiv auf eine antithrombotische Behandlung ansprechen als andere Tiere oder der Mensch. Aus den Versuchen ist zu entnehmen, daß eine Kombination von Dipyridamol und Acetalsalicylsäure die arterielle Thrombus-Bildung wesentlich wirksamer verhindert als eine Monotherapie. Die Überlegenheit der Behandlung mit einem Verhältnis von 100:1 gegenüber der mit einem Verhältnis von 10:1 bezüglich der Verhinderung der Thrombusbildung bestätigt die weiter oben genannten Ergebnisse bei Versuchen mit dem Mesenterialvenenmodell der Ratte.A combination of the two active substances intervenes in the first stage of thrombus formation; the risk of recurrent thrombosis in a system with high pressure and high flow and shear rates ("high flow / high pressure" system) is significantly reduced. The preferred dose (in rabbits) is 50: 1 (dipyridamole to acetylsalicylic acid). However, one should not forget that rabbits are generally less sensitive to antithrombotic treatment than other animals or humans. It can be seen from the experiments that a combination of dipyridamole and acetalsalicylic acid prevents arterial thrombus formation much more effectively than monotherapy. The superiority of the treatment with a ratio of 100: 1 over that with a ratio of 10: 1 in preventing thrombus formation confirms the results mentioned above in experiments with the rat mesenteric vein model.
Die folgenden Beispiele sollen die Erfindung nähers erläutern:The following examples are intended to illustrate the invention:
35 kg Dipyridamol, 30 kg Fumarsäure und 5 kg Polyvinylpyrrolidon mischt man 15 Minuten in einem Kubusmischer. Man mischt 0,4 kg Magnesiumstearat zu und mischt nochmals für 5 Minuten.35 kg of dipyridamole, 30 kg of fumaric acid and 5 kg of polyvinylpyrrolidone are mixed in a cube mixer for 15 minutes. 0.4 kg of magnesium stearate are mixed in and mixed again for 5 minutes.
Die Mischung gibt man über einen Walzenkompaktor, dem ein Trockengranuliergerät mit Siebeinrichtung nachgeschaltet ist. Verwendung findet die Fraktion von 0,4 bis 1,0 mm Durchmesser.The mixture is passed through a roller compactor, which is followed by a dry pelletizer with a screening device. The fraction from 0.4 to 1.0 mm in diameter is used.
35 kg O-Acetylsalicylsäure(kristallin) werden mit 3,3 kg fließfähiger Lactose, 12,5 kg mikrokristalliner Cellulose, 9 kg getrockneter Maisstärke und 0,5 kg Aluminiumstearat in einem Kubusmischer 15 Minuten gemischt und dann zu 90 mg schweren, bikonvexen Tabletten mit einem Durchmesser von 5,5 mm verpreßt.35 kg of O-acetylsalicylic acid (crystalline) are mixed with 3.3 kg of flowable lactose, 12.5 kg of microcrystalline cellulose, 9 kg of dried corn starch and 0.5 kg of aluminum stearate in a cube mixer for 15 minutes and then mixed with 90 mg, biconvex tablets pressed with a diameter of 5.5 mm.
Diese Kerne überzieht man in mehreren Schritten mit einer Dragiersuspension, bestehend aus 5,6 kg Saccharose, 0,5 kg Gummi arabicum und 3,8 kg Talcum bis die Tabletten ein Gewicht von 110 mg haben. Die Dragées werden gut getrocknet.These pits are coated in several steps with a coating suspension consisting of 5.6 kg sucrose, 0.5 kg gum arabic and 3.8 kg talc until the tablets have a weight of 110 mg. The dragées are dried well.
Auf einer Spezialkapselmaschine füllt man in eine Hartgelatine-Kapsel der Größe 1 die 175 mg Dipyridamol entsprechende Granulatmenge ein und legt dann das 35 mg O-Acetylsalicylsäure enthaltende Dragée obenauf. Das Gewichtsverhältnis Dipyridamol zu O-Acetylsalicylsäure beträgt 5.On a special capsule machine, the quantity of granules corresponding to 175 mg of dipyridamole is filled into a hard gelatin capsule of
300 kg ausgerundete Weinsäure-Starterpellets werden in einem Spezialkessel mit einer Suspension bestehend aus Isopropanol, Dipyridamol und Polyvinylpyrrolidon solange besprüht, bis die entstehenden Wirkstoffpellets ca. 45% Dipyridamol enthalten.300 kg of rounded tartaric acid starter pellets are sprayed in a special kettle with a suspension consisting of isopropanol, dipyridamole and polyvinylpyrrolidone until the resulting active substance pellets contain approximately 45% dipyridamole.
Diese Pellets besprüht man mit einem Lack, der aus Methacrylsäure/Methylmethacrylat-Copolymer (Handelsname Eudragit S) und Hydroxypropylmethylcellulosephthalat (Handelsname HP 55) im Gewichtsverhältnis 85:15 bis 50:50 besteht. Die organischen Lacklösungen enthalten noch Weichmacher und Talkum. Es werden zwei Pelletkomponenten mit 5 und 7% Hüllenanteil und unterschiedlichem Verhältnis der Lackkomponenten in den genannten Grenzen gesprüht. Die beiden Komponenten werden so gemischt, daß sie nachfolgende in vitro Freigabe ergeben:These pellets are sprayed with a lacquer consisting of methacrylic acid / methyl methacrylate copolymer (trade name Eudragit S) and hydroxypropylmethyl cellulose phthalate (trade name HP 55) in a weight ratio of 85:15 to 50:50. The organic paint solutions also contain plasticizers and talc. Two pellet components with 5 and 7% casing content and different ratios of the lacquer components are sprayed within the stated limits. The two components are mixed so that they give the following in vitro release:
Bedingungen: entsprechend US P XXI, Basket-Methode, 100 Umdrehungen/Min.
1 Stunde künstlicher Magensaft,
2 bis 6 Stunden künstlicher Darmsaft (Phosphatpuffer pH 5,5)Conditions: according to US P XXI, basket method, 100 revolutions / min.
1 hour of artificial gastric juice,
2 to 6 hours of artificial intestinal juice (phosphate buffer pH 5.5)
- 1. Stunde ca. 30 %1st hour approx. 30%
- 2. Stunde ca. 25 %2nd hour approx. 25%
- 3. Stunde ca. 18 %3rd hour approx. 18%
- 4. Stunde ca. 12 %4th hour approx. 12%
nach der 6. Stunde mehr als 90 % Dipyridamol-Freigabe.after the 6th hour more than 90% dipyridamole release.
Wie im Beispiel 1 beschrieben werden 100 mg schwere Acetylsalicylsäure-Kerne durch Verpressung folgender Mischung hergestellt:
O-Acetylsalicylsäure 25,0 Gew.-%
Lactose 53,0 Gew.-%
Mikrokristalline Cellulose 11,0 Gew.-%
Maisstärke, getrocknet 8,6 Gew.-%
Siliciumdioxid 3,0Gew.-%
Aluminiumstearat 0,4 Gew.-%As described in Example 1, 100 mg acetylsalicylic acid cores are produced by pressing the following mixture:
O-acetylsalicylic acid 25.0% by weight
Lactose 53.0% by weight
Microcrystalline cellulose 11.0% by weight
Corn starch, dried 8.6% by weight
Silicon dioxide 3.0% by weight
Aluminum stearate 0.4% by weight
Diese Kerne werden wie beschrieben solange mit der genannten Dragiersuspension überzogen, bis sie nach guter Trocknung 120 mg wiegen.As described, these kernels are coated with the coating suspension mentioned until they weigh 120 mg after thorough drying.
Auf einer Spezial-Kapselmaschine werden in eine Kapsel, Größe O, die 200 mg Dipyridamol entsprechende Pellet-Menge und ein 25 mg Acetylsalicylsäure enthaltendes Dragée eingefüllt.On a special capsule machine, a size O capsule, the amount of pellet corresponding to 200 mg of dipyridamole and a dragée containing 25 mg of acetylsalicylic acid are filled.
Das Gewichtsverhältnis Dipyridamol zu O-Acetylsalicylsäure beträgt 8.The weight ratio of dipyridamole to O-acetylsalicylic acid is 8.
In einem Doppelschneckenextruder werden ein Dipyridamol enthaltendes Pulvergemisch und ein organisches Lösungsmittel im richtigen Verhältnis hineindosiert und miteinander vermischt. Die befeuchtete Masse wird in Form von Spaghettis ausgedrückt, die in einem Behälter mit einer schnell drehenden Bodenplatte zu hoch verdichteten Pellets gerundet werden. Die Pellets trocknet man anschließend in einem Trockenschrank.In a twin-screw extruder, a powder mixture containing dipyridamole and an organic solvent are metered in in the correct ratio and mixed together. The moistened mass is expressed in the form of spaghetti, which are rounded into highly compacted pellets in a container with a rapidly rotating base plate. The pellets are then dried in a drying cabinet.
Dipyridamol 69,0 Gew.-%
Äthylcellulose 5,5 Gew.-%
Hydroxypropylmethylcellulose, hochpolymer 12,5 Gew.-%
Polyäthylenglykol 6000 1,0 Gew.-%
Fumarsäure 12,0 Gew.-%
Dipyridamole 69.0% by weight
Ethyl cellulose 5.5% by weight
Hydroxypropylmethyl cellulose, high polymer 12.5% by weight
Polyethylene glycol 6000 1.0% by weight
Fumaric acid 12.0% by weight
Wie in den Beispielen 1 und 2 beschrieben stellt man unter Verwendung der gleichen Hilfsstoffe ein 75 mg schweres Acetylsalicylsäure-Dragée her, das 5 mg dieses Stoffes enthält.As described in Examples 1 and 2, a 75 mg acetylsalicylic acid tablet containing 5 mg of this substance is produced using the same auxiliary substances.
Auf einer Spezial-Kapselmaschine werden in eine Kapsel der Größe OO eine Pelletmenge, die 450 mg Dipyridamol entspricht, und ein 5 mg Acetylsalicylsäure enthaltendes Dragée eingefüllt.On a special capsule machine, a pellet quantity corresponding to 450 mg dipyridamole and a dragée containing 5 mg acetylsalicylic acid are filled into a capsule of size OO.
Das Gewichtsverhältnis Dipyridamol zu O-Acetylsalicylsäure beträgt 90.The weight ratio of dipyridamole to O-acetylsalicylic acid is 90.
Für eine 3-Schicht-Tablette werden 3 Granulate hergestellt:3 granules are produced for a 3-layer tablet:
Eine Pulvermischung aus 80% Dipyridamol, 10% Hydroxypropylmethylcellulose (hochpolymer) und 9,5% Hydroxypropylcellulose (hochpolymer) werden in einem Granuliergerät mit Äthanol befeuchtet und durch ein Sieb mit Maschenweite 1,5 mm granuliert. Nach Trocknung und Siebung mischt man 0,5% Magnesiumstearat zu (prozentuale Angaben in Gew.-%).A powder mixture of 80% dipyridamole, 10% hydroxypropylmethyl cellulose (high polymer) and 9.5% hydroxypropyl cellulose (high polymer) are moistened with ethanol in a granulator and granulated through a sieve with a mesh size of 1.5 mm. After drying and sieving, 0.5% magnesium stearate is mixed in (percentages in% by weight).
Eine Mischung aus 50% Lactose und 45% mikrokristalliner Cellulose wird mit 4,5% Polyvinylpyrrolidon, gelöst in Wasser, befeuchtet. Das durch ein Sieb der Maschenweite 1 mm gesiebte Granulat wird getrocknet und mit 0,5% Aluminiumstearat gemischt (prozentuale Angaben in Gew.-%).A mixture of 50% lactose and 45% microcrystalline cellulose is moistened with 4.5% polyvinylpyrrolidone, dissolved in water. The granulate sieved through a sieve with a mesh size of 1 mm is dried and mixed with 0.5% aluminum stearate (percentages in% by weight).
80% fließfähige Acetylsalicylsäure-Kristalle werden mit 15% fließfähiger Lactose, 4,5% mikrokristalliner Cellulose und 0,5% Aluminiumstearat gemischt (prozentuale Angaben in Gew.-%).80% flowable acetylsalicylic acid crystals are mixed with 15% flowable lactose, 4.5% microcrystalline cellulose and 0.5% aluminum stearate (percentages in% by weight).
Auf einer Spezial-Tablettenpresse mit 3 Fülltrichtern und 3 Preßstationen werden die Granulate so zudosiert, daß eine Tablette mit 400 mg Dipyridamol und 80 mg Acetylsalicylsäure entsteht. Die neutrale Schicht zwischen den beiden Wirkstoffen wiegt 50 mg. Die Tablette in Oblong-Form (17×6,8 mm) wird gut entstaubt, nachgetrocknet und in Aluminium/Aluminium-Blisterstreifen eingesiegelt.The granules are metered in on a special tablet press with 3 filling funnels and 3 pressing stations so that a tablet with 400 mg dipyridamole and 80 mg acetylsalicylic acid is formed. The neutral layer between the two active substances weighs 50 mg. The tablet in oblong form (17 × 6.8 mm) is dedusted well, dried and sealed in aluminum / aluminum blister strips.
Das Gewichtsverhältnis Dipyridamol zu O-Acetylsalicylsäure beträgt 5.The weight ratio of dipyridamole to O-acetylsalicylic acid is 5.
Eine Mischung aus 30% Dipyridamol, 63% Fumarsäure und 6% Polyvinylpyrrolidon wird mit Äthanol befeuchtet und durch ein Sieb mit einer Maschenweite von 1,5 mm gesiebt. Nach Trocknung mischt man 1% Magnesiumstearat zu und verdichtet das Granulat auf einem Walzenkompaktor, der mit einem Trockengranuliergerät mit Siebeinrichtung ausgstattet ist.A mixture of 30% dipyridamole, 63% fumaric acid and 6% polyvinylpyrrolidone is moistened with ethanol and sieved through a sieve with a mesh size of 1.5 mm. After drying, 1% of magnesium stearate is added and the granules are compacted on a roller compactor equipped with a dry granulator with a sieve.
Die Fraktion der Korngröße von 0,4 bis 1,25 mm wird weiterverwendet (prozentuale Angaben in Gew.-%).The fraction of the grain size from 0.4 to 1.25 mm is used further (percentages in% by weight).
Auf einer Spezial-Kapselmaschine werden in eine Kapsel, Größe O, die 100 mg Dipyridamol entsprechende Menge an Granulat und ein 5 mg Acetylsalicylsäure enthaltendes Dragée entsprechend Beispiel 3 eingefüllt.On a special capsule machine, a size O capsule, the amount of granules corresponding to 100 mg of dipyridamole and a dragée containing 5 mg of acetylsalicylic acid according to Example 3 are introduced.
Die Wirkstofffreigabe des Dipyridamol-enthaltenden Granulates ist pH-unabhängig:
Das Gewichtsverhältnis von Dipyridamol zu O-Acetylsalicylsäure beträgt 20.The weight ratio of dipyridamole to O-acetylsalicylic acid is 20.
35 kg Mopidamol, 20 kg Fumarsäure und 5 kg Polyvinylpyrrolidon mischt man 15 Minuten in einem Kubusmischer. Man mischt 0,4 kg Magnesiumstearat zu und mischt nochmals für 5 Minuten.35 kg of mopidamol, 20 kg of fumaric acid and 5 kg of polyvinylpyrrolidone are mixed in a cube mixer for 15 minutes. 0.4 kg of magnesium stearate are mixed in and mixed again for 5 minutes.
Die Mischung gibt man über einen Walzenkompaktor, dem ein Trockengranuliergerät mit Siebeinrichtung nachgeschaltet ist. Verwendung findet die Fraktion von 0,4 bis 1,0 mm Durchmesser.The mixture is passed through a roller compactor, which is followed by a dry pelletizer with a screening device. The fraction from 0.4 to 1.0 mm in diameter is used.
35 kg O-Acetylsalicylsäure(kristallin) werden mit 3,3 kg fließfähiger Lactose, 12,5 kg mikrokristalliner Cellulose, 9 kg getrockneter Maisstärke und 0,5 kg Aluminiumstearat in einem Kubusmischer 15 Minuten gemischt und dann zu 90 mg schweren, bikonvexen Tabletten mit einem Durchmesser von 5,5 mm verpreßt.35 kg of O-acetylsalicylic acid (crystalline) are mixed with 3.3 kg of flowable lactose, 12.5 kg of microcrystalline cellulose, 9 kg of dried corn starch and 0.5 kg of aluminum stearate in a cube mixer for 15 minutes and then mixed with 90 mg, biconvex tablets pressed with a diameter of 5.5 mm.
Diese Kerne überzieht man in mehreren Schritten mit einer Dragiersuspension, bestehend aus 5,6 kg Saccharose, 0,5 kg Gummi arabicum und 3,8 kg Talcum bis die Tabletten ein Gewicht von 110 mg haben. Die Dragées werden gut getrocknet.These pits are coated in several steps with a coating suspension consisting of 5.6 kg sucrose, 0.5 kg gum arabic and 3.8 kg talc until the tablets have a weight of 110 mg. The dragées are dried well.
Auf einer Spezialkapselmaschine füllt man in eine Hartgelatine-Kapsel der Größe 1 die 210 mg Mopidamol entsprechende Granulatmenge ein und legt dann das 35 mg O-Acetylsalicylsäure enthaltende Dragée obenauf. Das Gewichtsverhältnis Mopidamol zu O-Acetylsalicylsäure beträgt 6.On a special capsule machine, fill the hard gelatin capsule with
Claims (10)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT87111104T ATE59961T1 (en) | 1986-08-13 | 1987-07-31 | MEDICATIONS CONTAINING DIPYRIDAMOL OR MOPIDAMOL AND O-ACETYLSALICYLIC ACID OR. THEIR PHYSIOLOGICALLY TOLERABLE SALTS, PROCESSES FOR THEIR PRODUCTION AND THEIR USE TO COMBAT THE FORMATION OF THROMBUS. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3627423 | 1986-08-13 | ||
DE19863627423 DE3627423A1 (en) | 1986-08-13 | 1986-08-13 | MEDICINAL PRODUCTS CONTAINING DIPYRIDAMOL OR MOPIDAMOL AND O-ACETYLSALICYL ACID OR THEIR PHYSIOLOGICALLY COMPATIBLE SALTS, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR COMBATING THROMBUS FORMATION |
Publications (2)
Publication Number | Publication Date |
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EP0257344A1 true EP0257344A1 (en) | 1988-03-02 |
EP0257344B1 EP0257344B1 (en) | 1991-01-16 |
Family
ID=6307286
Family Applications (1)
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EP87111104A Expired - Lifetime EP0257344B1 (en) | 1986-08-13 | 1987-07-31 | Medicaments containing dipyridamol or mopidamol and o-acetylsalicylic acid, or its physiologically compatible salts, process for their manufacture and their use in combating the formation of thrombus |
Country Status (26)
Country | Link |
---|---|
US (1) | US6015577A (en) |
EP (1) | EP0257344B1 (en) |
JP (1) | JP2593879B2 (en) |
KR (1) | KR950009098B1 (en) |
AT (1) | ATE59961T1 (en) |
AU (1) | AU603146B2 (en) |
BR (1) | BR1100593A (en) |
CA (1) | CA1302272C (en) |
CL (1) | CL2004001252A1 (en) |
DD (1) | DD263918A5 (en) |
DE (3) | DE3627423A1 (en) |
DK (1) | DK172236B1 (en) |
ES (1) | ES2020974B3 (en) |
FI (1) | FI873492A (en) |
GR (1) | GR3001695T3 (en) |
HK (1) | HK14494A (en) |
HU (1) | HU202404B (en) |
IE (1) | IE60862B1 (en) |
IL (1) | IL83510A (en) |
NL (1) | NL990001I2 (en) |
NO (2) | NO175132C (en) |
NZ (1) | NZ221424A (en) |
PH (1) | PH27176A (en) |
PT (1) | PT85525B (en) |
SG (1) | SG122593G (en) |
ZA (1) | ZA875947B (en) |
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WO2009118321A1 (en) * | 2008-03-28 | 2009-10-01 | Boehringer Ingelheim International Gmbh | Method for manufacturing acid pellets |
WO2010036975A2 (en) * | 2008-09-25 | 2010-04-01 | Teva Pharmaceutical Industries Ltd. | Dipyridamole and acetylsalicylic acid formulations and process for preparing same |
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FR2368272A1 (en) * | 1976-10-20 | 1978-05-19 | Theramex | Solid aspirin-dipyridamole compsns. - each sepd. from other by inert material, for reducing platelet aggregation |
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DE3000979A1 (en) * | 1980-01-12 | 1981-07-23 | Dr. Karl Thomae Gmbh, 7950 Biberach | NEW DIPYRIDAMOL RETARD FORMS AND METHOD FOR THEIR PRODUCTION |
FR2513118A1 (en) * | 1981-09-18 | 1983-03-25 | Rocador Sa | PHARMACEUTICAL COMPOSITION BASED ON DIPYRIDAMOL AND ALUMINUM SALT OF ACETYLSALICYLIC ACID TO COMBAT PLATELET AGGREGATION |
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1986
- 1986-08-13 DE DE19863627423 patent/DE3627423A1/en not_active Withdrawn
-
1987
- 1987-07-31 DE DE2002199015 patent/DE10299015I2/en active Active
- 1987-07-31 EP EP87111104A patent/EP0257344B1/en not_active Expired - Lifetime
- 1987-07-31 DE DE8787111104T patent/DE3767408D1/en not_active Expired - Lifetime
- 1987-07-31 AT AT87111104T patent/ATE59961T1/en active
- 1987-07-31 ES ES87111104T patent/ES2020974B3/en not_active Expired - Lifetime
- 1987-08-11 PH PH35653A patent/PH27176A/en unknown
- 1987-08-11 CA CA000544180A patent/CA1302272C/en not_active Expired - Lifetime
- 1987-08-11 DD DD87305901A patent/DD263918A5/en not_active IP Right Cessation
- 1987-08-12 PT PT85525A patent/PT85525B/en unknown
- 1987-08-12 DK DK421187A patent/DK172236B1/en not_active IP Right Cessation
- 1987-08-12 AU AU76795/87A patent/AU603146B2/en not_active Expired
- 1987-08-12 JP JP62201688A patent/JP2593879B2/en not_active Expired - Lifetime
- 1987-08-12 IE IE215287A patent/IE60862B1/en not_active IP Right Cessation
- 1987-08-12 ZA ZA875947A patent/ZA875947B/en unknown
- 1987-08-12 FI FI873492A patent/FI873492A/en not_active Application Discontinuation
- 1987-08-12 HU HU873652A patent/HU202404B/en unknown
- 1987-08-12 NO NO873370A patent/NO175132C/en not_active IP Right Cessation
- 1987-08-12 IL IL83510A patent/IL83510A/en not_active IP Right Cessation
- 1987-08-12 NZ NZ221424A patent/NZ221424A/en unknown
- 1987-08-13 KR KR87008873A patent/KR950009098B1/en not_active IP Right Cessation
-
1991
- 1991-03-29 GR GR91400406T patent/GR3001695T3/en unknown
-
1993
- 1993-11-11 SG SG122593A patent/SG122593G/en unknown
-
1994
- 1994-02-24 HK HK144/94A patent/HK14494A/en not_active IP Right Cessation
-
1995
- 1995-04-12 US US08/421,351 patent/US6015577A/en not_active Expired - Lifetime
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1997
- 1997-05-13 BR BR1100593-9A patent/BR1100593A/en active IP Right Grant
-
1999
- 1999-01-06 NL NL990001C patent/NL990001I2/en unknown
- 1999-07-01 NO NO1999014C patent/NO1999014I1/en unknown
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2004
- 2004-05-24 CL CL200401252A patent/CL2004001252A1/en unknown
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Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1733729A1 (en) | 2003-02-13 | 2006-12-20 | Boehringer Ingelheim International Gmbh | Use of dipyridamole in combination with acetylsalicylic acid and an angiotensin ii antagonist for stroke prevention |
EP2062580A1 (en) | 2003-04-24 | 2009-05-27 | Boehringer Ingelheim International GmbH | Use of dipyridamole or mopidamole for treatment and prevention of thromboembolic diseases and disorders caused by excessive formation of thrombin and/or by elevated expression of trombin receptors |
WO2005113006A3 (en) * | 2004-05-13 | 2007-02-08 | Boehringer Ingelheim Int | Use of dipyridamole for treatment of resistance to platelet inhibitors |
WO2009118321A1 (en) * | 2008-03-28 | 2009-10-01 | Boehringer Ingelheim International Gmbh | Method for manufacturing acid pellets |
US10251840B2 (en) | 2008-03-28 | 2019-04-09 | Boehringer Ingelheim International Gmbh | Method for manufacturing acid pellets |
WO2010036975A2 (en) * | 2008-09-25 | 2010-04-01 | Teva Pharmaceutical Industries Ltd. | Dipyridamole and acetylsalicylic acid formulations and process for preparing same |
WO2010036975A3 (en) * | 2008-09-25 | 2010-08-12 | Teva Pharmaceutical Industries Ltd. | Dipyridamole and acetylsalicylic acid formulations and process for preparing same |
EP2361615A1 (en) | 2010-02-19 | 2011-08-31 | Alfred E. Tiefenbacher GmbH & Co. KG | Dipyridamole prolonged-release tablet |
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